[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"site-settings":3,"footer-product-categories":40,"header-product-categories":199,"blog-cara-memilih-pass-box-cleanroom-farmasi-makanan-2026--":237,"blog-recent":273},{"data":4},{"business_hours":5,"canonical_url":6,"catalog_full_url":7,"catalog_price_url":7,"catalog_technical_url":7,"contact_address":8,"contact_email":9,"contact_factory_address":10,"contact_factory_map_url":11,"contact_office_address":7,"contact_phone":12,"contact_whatsapp":13,"custom_body_scripts":7,"custom_head_scripts":14,"ga_measurement_id":15,"google_ads_id":16,"gtm_id":17,"homepage_meta_description_en":18,"homepage_meta_description_id":19,"homepage_meta_description_zh":20,"homepage_meta_title_en":21,"homepage_meta_title_id":22,"homepage_meta_title_zh":23,"maintenance_message":7,"maintenance_mode":24,"meta_description_default":25,"meta_title_default":26,"og_image_default":27,"recaptcha_site_key":7,"robots_txt":28,"schema_org_founded":29,"schema_org_type":30,"seo_noindex":24,"site_email":9,"site_favicon_url":31,"site_logo_url":32,"site_name":33,"site_stats":34,"site_tagline":35,"social_facebook":36,"social_instagram":37,"social_linkedin":7,"social_youtube":38,"whatsapp_message":39,"whatsapp_number":12},"Senin-Sabtu 08:00-17:00 WIB","https://sandwichpanels.id","","Jakarta, Indonesia","marketing@sandwichpanels.id","Kawasan Industri Lippo Cikarang Delta Silicon, Jl. Albasia Utara 1, Cikarang Selatan, Jawa Barat, Indonesia, 17550","https://maps.google.com/?q=-6.3666492909764205, 107.12342048001176","+628119898835","628119898835","\u003Cmeta name=\"google-site-verification\" content=\"tjwEbF9G67SnEcroXL7PBzxRcLoD0NaRxKXRgRvOV6o\" />","G-DPYQT7JZ2D","G-ETSSTN3J3T","GTM-5XRVSZWC","SandwichPanels.id supplies EPS, PU, PIR, and rockwool sandwich panels for factories, cold rooms, cleanrooms, and industrial buildings in Indonesia.","SandwichPanels.id menyediakan sandwich panel EPS, PU, PIR, dan rockwool untuk pabrik, cold storage, cleanroom, dan bangunan industri di Indonesia.","SandwichPanels.id 为印度尼西亚工厂、冷库、洁净室与工业建筑提供 EPS、PU、PIR 和岩棉夹芯板解决方案。","Sandwich Panels Indonesia for Cold Rooms and Factories","Sandwich Panel Indonesia untuk Pabrik, Cold Room, Cleanroom","印度尼西亚工厂、冷库与洁净室夹芯板","false","Supplier sandwich panel EPS, PU, PIR, dan rockwool untuk pabrik, cold storage, cleanroom, dan bangunan industri di Indonesia.","Sandwich Panel Indonesia untuk Pabrik & 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Panel","夹芯板配件",37,"sandwich-panel-accessories",{"data":200},[201,203,205,207,209,211,213,215,217,219,221,223,225,227,229,231,233,235],{"id":43,"image_url":44,"name":202,"position":49,"slug":50,"type":51},{"en":46,"id":47,"zh":48},{"id":53,"image_url":54,"name":204,"position":59,"slug":60,"type":51},{"en":56,"id":57,"zh":58},{"id":62,"image_url":63,"name":206,"position":68,"slug":69,"type":51},{"en":65,"id":66,"zh":67},{"id":71,"image_url":72,"name":208,"position":77,"slug":78,"type":51},{"en":74,"id":75,"zh":76},{"id":80,"image_url":81,"name":210,"position":85,"slug":86,"type":51},{"en":83,"id":83,"zh":84},{"id":88,"image_url":89,"name":212,"position":94,"slug":95,"type":51},{"en":91,"id":92,"zh":93},{"id":97,"image_url":7,"name":214,"position":102,"slug":103,"type":51},{"en":99,"id":100,"zh":101},{"id":105,"image_url":106,"name":216,"position":111,"slug":112,"type":51},{"en":108,"id":109,"zh":110},{"id":114,"image_url":115,"name":218,"position":120,"slug":121,"type":51},{"en":117,"id":118,"zh":119},{"id":123,"image_url":115,"name":220,"position":127,"slug":128,"type":51},{"en":125,"id":125,"zh":126},{"id":130,"image_url":131,"name":222,"position":136,"slug":137,"type":51},{"en":133,"id":134,"zh":135},{"id":139,"image_url":7,"name":224,"position":144,"slug":145,"type":51},{"en":141,"id":142,"zh":143},{"id":147,"image_url":148,"name":226,"position":153,"slug":154,"type":51},{"en":150,"id":151,"zh":152},{"id":156,"image_url":157,"name":228,"position":162,"slug":163,"type":51},{"en":159,"id":160,"zh":161},{"id":165,"image_url":166,"name":230,"position":171,"slug":172,"type":51},{"en":168,"id":169,"zh":170},{"id":174,"image_url":175,"name":232,"position":180,"slug":181,"type":51},{"en":177,"id":178,"zh":179},{"id":183,"image_url":184,"name":234,"position":188,"slug":189,"type":51},{"en":186,"id":186,"zh":187},{"id":191,"image_url":192,"name":236,"position":197,"slug":198,"type":51},{"en":194,"id":195,"zh":196},{"author_name":238,"category":239,"content":241,"cover_image":245,"created_at":246,"excerpt":247,"id":251,"published":252,"published_at":253,"seo":254,"slug":263,"tags":264,"title":272,"updated_at":246},"Administrator",{"name":240,"slug":95},{"en":91,"id":92,"zh":93},{"en":242,"id":243,"zh":244},"\u003Ch2>What Is a Pass Box and Why It Matters for Pharma & Food Cleanrooms\u003C/h2>\n\n\u003Cp>A pass box — also known as a \u003Cem>pass-through chamber\u003C/em> or \u003Cem>transfer hatch\u003C/em> — is a material transfer device between cleanroom zones, designed to minimize cross-contamination. It is a critical component in pharmaceutical and food industry facilities that must comply with \u003Cstrong>ISO 14644\u003C/strong> and \u003Cstrong>GMP (Good Manufacturing Practice)\u003C/strong> standards.\u003C/p>\n\n\u003Cp>In pharmaceutical cleanrooms, every transfer of raw materials, test samples, or production equipment between different cleanliness zones (e.g., ISO 8 to ISO 7) must go through a pass box. Without the right pass box, opening doors between rooms directly can cause particle level spikes and BPOM audit failures.\u003C/p>\n\n\u003Cp>For the food industry, pass boxes prevent microbiological contamination when moving ingredients from preparation areas to sterile packaging zones. Data from the \u003Cstrong>FDA Food Safety Modernization Act\u003C/strong> indicates that 23% of food product recalls are linked to contamination control failures during material transfer processes.\u003C/p>\n\n\u003Cp>Choosing the right pass box goes beyond buying a stainless steel box — technical specifications must match your cleanroom classification, the materials being transferred, and your usage frequency. See also our comprehensive guide on \u003Ca href=\"/artikel/bahan-dinding-cleanroom-panduan-lengkap\">cleanroom wall materials\u003C/a> for a full understanding of the cleanroom equipment ecosystem.\u003C/p>\n\n\u003Cimg src=\"https://assets.sandwichpanels.id/blog/1783058576170-20260703-060256-pass-box-dinamis-diagram-01.jpg\" alt=\"Dynamic pass box diagram with HEPA filter and airflow between cleanroom zones\" loading=\"lazy\" />\n\n\u003Ch2>Types of Pass Boxes: Static, Dynamic, and UV\u003C/h2>\n\n\u003Cp>Generally, cleanroom pass boxes fall into three main categories:\u003C/p>\n\n\u003Ch3>1. Static Pass Box\u003C/h3>\n\u003Cp>A static pass box has no active air filtration system. It is suitable for transfers between rooms with \u003Cstrong>the same ISO classification\u003C/strong> or from a cleaner zone to a less clean zone. Lower cost and minimal maintenance, but not recommended for transfers from contaminated areas to sterile areas without manual cleaning procedures. Learn the differences in detail in our article on \u003Ca href=\"/artikel/pass-box-statis-vs-dinamis-cleanroom-panduan-memilih\">static vs dynamic pass boxes\u003C/a>.\u003C/p>\n\n\u003Ch3>2. Dynamic Pass Box\u003C/h3>\n\u003Cp>Equipped with a \u003Cstrong>HEPA filter and blower\u003C/strong> that continuously supplies clean air into the chamber. A dynamic pass box is mandatory when transferring materials from a lower ISO zone to a higher ISO zone (e.g., ISO 8 to ISO 7). The HEPA-filtered air creates positive pressure that prevents external particles from entering.\u003C/p>\n\n\u003Ch3>3. UV Pass Box\u003C/h3>\n\u003Cp>Equipped with a \u003Cstrong>UV-C germicidal lamp (254 nm)\u003C/strong> for surface sterilization of transferred items. Essential for pharmaceutical facilities handling sterile materials and food industries requiring packaging decontamination. UV exposure typically lasts 15–30 minutes per cycle, with an \u003Cem>interlock safety\u003C/em> feature that prevents the door from opening while UV is active.\u003C/p>\n\n\u003Ch2>ISO 14644 and GMP Standards to Meet\u003C/h2>\n\n\u003Cp>Pass boxes for pharmaceutical and food industries must comply with strict requirements:\u003C/p>\n\n\u003Cul>\n  \u003Cli>\u003Cstrong>ISO 14644-1:2015\u003C/strong> — Air cleanliness classification based on particle concentration. The pass box must maintain room classification on both sides without adding contamination.\u003C/li>\n  \u003Cli>\u003Cstrong>ISO 14644-3:2019\u003C/strong> — Cleanroom test methods including \u003Cem>filter leakage test\u003C/em> and \u003Cem>airflow velocity test\u003C/em> for dynamic pass boxes.\u003C/li>\n  \u003Cli>\u003Cstrong>GMP Annex 1 (EU)\u003C/strong> — Requires interlocked pass boxes for sterile production facilities, with routine validation of UV effectiveness and filter integrity.\u003C/li>\n  \u003Cli>\u003Cstrong>CPOB 2018 (BPOM Indonesia)\u003C/strong> — Good Manufacturing Practice guidelines in Indonesia mandate validated and documented material transfer systems.\u003C/li>\n\u003C/ul>\n\n\u003Cp>A standards-compliant pass box should come with material certificates, filter leak test reports (DOP/PAO test), and operational validation protocols.\u003C/p>\n\n\u003Ch2>Pass Box Materials: Stainless Steel vs Other Options\u003C/h2>\n\n\u003Cp>The construction material of the pass box significantly affects durability, cleanability, and resistance to cleaning chemicals:\u003C/p>\n\n\u003Ctable>\n  \u003Ctr>\u003Cth>Material\u003C/th>\u003Cth>Advantages\u003C/th>\u003Cth>Disadvantages\u003C/th>\u003Cth>Suitable For\u003C/th>\u003C/tr>\n  \u003Ctr>\u003Ctd>\u003Cstrong>SS304\u003C/strong>\u003C/td>\u003Ctd>Corrosion-resistant, easy to clean, food-grade\u003C/td>\u003Ctd>Mid-range cost\u003C/td>\u003Ctd>Standard pharma & food cleanrooms\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>\u003Cstrong>SS316L\u003C/strong>\u003C/td>\u003Ctd>Acid & chloride resistant, electropolished surface\u003C/td>\u003Ctd>Higher cost\u003C/td>\u003Ctd>Sterile pharma, aggressive chemicals\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>\u003Cstrong>Powder Coated Steel\u003C/strong>\u003C/td>\u003Ctd>Economical\u003C/td>\u003Ctd>Scratch-prone, not resistant to strong disinfectants\u003C/td>\u003Ctd>Non-critical areas only\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>\u003Cstrong>PVC/Plastic\u003C/strong>\u003C/td>\u003Ctd>Lightweight, anti-static\u003C/td>\u003Ctd>Less rigid\u003C/td>\u003Ctd>ESD areas, electronics industry\u003C/td>\u003C/tr>\n\u003C/table>\n\n\u003Cp>For pharmaceutical and food cleanrooms, \u003Cstrong>SS304 at minimum\u003C/strong> — and SS316L if the process involves aggressive disinfectants such as hydrogen peroxide vapor (HPV) or chlorine-based sanitizers.\u003C/p>\n\n\u003Ch2>Pass Box Sizes: Matching Your Transfer Needs\u003C/h2>\n\n\u003Cp>Pass box dimensions should be matched to the largest item being transferred. Common standard sizes available:\u003C/p>\n\n\u003Cul>\n  \u003Cli>\u003Cstrong>Small\u003C/strong>: 600 × 600 × 600 mm — for vials, ampoules, lab samples\u003C/li>\n  \u003Cli>\u003Cstrong>Medium\u003C/strong>: 800 × 800 × 800 mm — for raw material containers, small equipment\u003C/li>\n  \u003Cli>\u003Cstrong>Large\u003C/strong>: 1000 × 1000 × 1000 mm and above — for drums, packaging cartons, production equipment\u003C/li>\n  \u003Cli>\u003Cstrong>Custom\u003C/strong>: Tailored to specific cleanroom layout requirements\u003C/li>\n\u003C/ul>\n\n\u003Cp>Rule of thumb: internal dimensions should be at least \u003Cstrong>20% larger\u003C/strong> than the largest item to pass through, allowing easy loading and unloading without touching the chamber walls. For larger logistics needs, see our guide on \u003Ca href=\"/artikel/pass-box-logistik-material-handling-cleanroom-2026\">cleanroom pass boxes for logistics\u003C/a>.\u003C/p>\n\n\u003Ch2>Interlock Features: Preventing Cross-Contamination\u003C/h2>\n\n\u003Cp>The interlock system is the most critical safety mechanism on a pass box. Two types are available:\u003C/p>\n\n\u003Cul>\n  \u003Cli>\u003Cstrong>Mechanical Interlock\u003C/strong>: Uses cables and levers — both doors cannot physically open at the same time. Economical but requires periodic maintenance.\u003C/li>\n  \u003Cli>\u003Cstrong>Electromagnetic Interlock\u003C/strong>: Uses sensors and solenoid locks. Both doors are electronically locked; one door can only open when the other is fully closed. More reliable and mandatory for sterile pharmaceutical applications.\u003C/li>\n\u003C/ul>\n\n\u003Cp>Important additional features: \u003Cstrong>door status indicator\u003C/strong> (red/green LED), \u003Cstrong>automatic UV timer\u003C/strong>, and \u003Cstrong>emergency release\u003C/strong> for emergency situations. Ensure the interlock has been tested to IEC 61508 safety integrity standards.\u003C/p>\n\n\u003Ch2>Comparing Pass Box Requirements: Pharma vs Food Industry\u003C/h2>\n\n\u003Cp>Not all pass boxes are suitable for every industry. Here is a comparison of specific needs:\u003C/p>\n\n\u003Ctable>\n  \u003Ctr>\u003Cth>Aspect\u003C/th>\u003Cth>Pharma\u003C/th>\u003Cth>Food\u003C/th>\u003C/tr>\n  \u003Ctr>\u003Ctd>Cleanroom Classification\u003C/td>\u003Ctd>ISO 5–8 (Grade A–D)\u003C/td>\u003Ctd>ISO 7–8 generally\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>Pass Box Type\u003C/td>\u003Ctd>Dynamic + UV (mandatory for sterile)\u003C/td>\u003Ctd>Static with UV (sufficient for most cases)\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>Material\u003C/td>\u003Ctd>SS316L electropolished\u003C/td>\u003Ctd>SS304 food-grade\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>Validation\u003C/td>\u003Ctd>Full IQ/OQ/PQ, DOP test\u003C/td>\u003Ctd>Cleaning validation, swab test\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>Certification\u003C/td>\u003Ctd>BPOM CPOB, EU GMP Annex 1\u003C/td>\u003Ctd>HACCP, ISO 22000\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>UV Frequency\u003C/td>\u003Ctd>Every transfer cycle\u003C/td>\u003Ctd>Per batch or per shift\u003C/td>\u003C/tr>\n\u003C/table>\n\n\u003Ch2>Checklist: 7 Things to Check Before Buying a Pass Box\u003C/h2>\n\n\u003Col>\n  \u003Cli>\u003Cstrong>Target cleanroom classification\u003C/strong> — Determine the ISO class on both sides of the pass box. If there is more than a 1-level difference, a dynamic pass box is mandatory.\u003C/li>\n  \u003Cli>\u003Cstrong>Transfer material dimensions\u003C/strong> — Measure the maximum dimensions of items to be transferred; add a 20% margin.\u003C/li>\n  \u003Cli>\u003Cstrong>Construction material type\u003C/strong> — Ensure compatibility with the chemical resistance required against the disinfectants you use.\u003C/li>\n  \u003Cli>\u003Cstrong>Interlock system\u003C/strong> — Electromagnetic for critical applications; verify safety certification.\u003C/li>\n  \u003Cli>\u003Cstrong>Filtration\u003C/strong> — HEPA H13 minimum for dynamic pass boxes; check replacement filter availability locally.\u003C/li>\n  \u003Cli>\u003Cstrong>UV lamp\u003C/strong> — If needed, ensure UV intensity ≥ 200 μW/cm² and an hour-meter for scheduled replacement.\u003C/li>\n  \u003Cli>\u003Cstrong>Documentation and after-sales\u003C/strong> — Ensure the supplier provides FAT/SAT protocols, installation manuals, and local technical support.\u003C/li>\n\u003C/ol>\n\n\u003Ch2>Common Mistakes When Choosing a Pass Box and How to Avoid Them\u003C/h2>\n\n\u003Cp>Based on cleanroom project experience in Indonesia, here are the most frequent mistakes:\u003C/p>\n\n\u003Cul>\n  \u003Cli>\u003Cstrong>Choosing a static pass box for different-level zones\u003C/strong> — Consequence: ISO validation failure. Solution: always evaluate cleanroom pressure cascade before selecting the type.\u003C/li>\n  \u003Cli>\u003Cstrong>Ignoring interior material finish\u003C/strong> — Rough surfaces become particle accumulation points. Ensure Ra ≤ 0.8 μm for pharmaceutical applications.\u003C/li>\n  \u003Cli>\u003Cstrong>Not considering expansion\u003C/strong> — Buying a pass box that is too small. Purchase with a 30% capacity margin to anticipate production increases.\u003C/li>\n  \u003Cli>\u003Cstrong>Skipping FAT (Factory Acceptance Test)\u003C/strong> — Always request a FAT report before shipment, including filter leak test and interlock function test.\u003C/li>\n  \u003Cli>\u003Cstrong>No cleaning protocol\u003C/strong> — The pass box must be included in the cleanroom's routine cleaning schedule; document cleaning frequency and methods.\u003C/li>\n\u003C/ul>\n\n\u003Ch2>FAQ: Common Questions About Cleanroom Pass Boxes\u003C/h2>\n\n\u003Ch3>What's the difference between static and dynamic pass boxes for pharma cleanrooms?\u003C/h3>\n\u003Cp>A static pass box has no active filtration system and is suitable for same-ISO zones. A dynamic pass box is equipped with a HEPA filter and blower, mandatory when transferring from a lower ISO zone to a higher one. For sterile pharmaceutical production, a dynamic pass box is the minimum standard required by CPOB and EU GMP Annex 1.\u003C/p>\n\n\u003Ch3>Is UV light mandatory for cleanroom pass boxes?\u003C/h3>\n\u003Cp>Not always mandatory. UV light is required if you are transferring materials that need surface decontamination, such as sterile drug primary packaging or ready-to-eat food ingredients. For non-sterile applications, a pass box without UV can be used as long as manual cleaning procedures are consistently applied.\u003C/p>\n\n\u003Ch3>What's the ideal pass box size for the food industry?\u003C/h3>\n\u003Cp>For medium-scale food processing, a size of 800 × 800 × 800 mm is generally sufficient for transferring raw materials in standard containers. However, if you are moving drums or large cartons, consider 1000 × 1000 × 1000 mm or a custom size. Always add a 20% margin over the largest item dimension.\u003C/p>\n\n\u003Ch3>How to ensure the pass box meets GMP standards?\u003C/h3>\n\u003Cp>Ensure the pass box has: (1) material certificate for SS304/316L, (2) DOP/PAO test report for HEPA filter integrity (if dynamic), (3) validated interlock system, (4) complete IQ/OQ/PQ protocols, and (5) surface roughness ≤ 0.8 μm Ra for pharmaceutical applications. Request this documentation from the supplier before purchase.\u003C/p>","\u003Ch2>Apa Itu Pass Box dan Mengapa Penting untuk Cleanroom Farmasi & Makanan?\u003C/h2>\n\n\u003Cp>Pass box — juga dikenal sebagai \u003Cem>pass-through chamber\u003C/em> atau \u003Cem>transfer hatch\u003C/em> — adalah perangkat pemindah material antar ruangan cleanroom yang dirancang untuk meminimalkan kontaminasi silang. Alat ini menjadi komponen kritis dalam fasilitas farmasi dan industri makanan yang harus memenuhi standar \u003Cstrong>ISO 14644\u003C/strong> dan \u003Cstrong>GMP (Good Manufacturing Practice)\u003C/strong>.\u003C/p>\n\n\u003Cp>Dalam cleanroom farmasi, setiap transfer bahan baku, sampel uji, atau peralatan produksi antar zona kebersihan berbeda (misalnya dari ISO 8 ke ISO 7) harus melalui pass box. Tanpa pass box yang tepat, membuka pintu antar ruangan secara langsung dapat menyebabkan lonjakan partikel dan kegagalan audit BPOM.\u003C/p>\n\n\u003Cp>Untuk industri makanan, pass box berperan mencegah kontaminasi mikrobiologis saat memindahkan bahan dari area preparasi ke area pengemasan steril. Data dari \u003Cstrong>FDA Food Safety Modernization Act\u003C/strong> menunjukkan bahwa 23% kasus recall produk makanan terkait dengan kegagalan kontrol kontaminasi selama proses transfer material.\u003C/p>\n\n\u003Cp>Memilih pass box yang sesuai bukan sekadar membeli kotak stainless steel — ada spesifikasi teknis yang harus disesuaikan dengan klasifikasi cleanroom, jenis material yang ditransfer, dan frekuensi penggunaan. Baca juga panduan lengkap tentang \u003Ca href=\"/artikel/bahan-dinding-cleanroom-panduan-lengkap\">bahan dinding cleanroom\u003C/a> untuk memahami ekosistem peralatan cleanroom secara menyeluruh.\u003C/p>\n\n\u003Cimg src=\"https://assets.sandwichpanels.id/blog/1783058576170-20260703-060256-pass-box-dinamis-diagram-01.jpg\" alt=\"Diagram pass box dinamis dengan HEPA filter dan aliran udara antar zona cleanroom\" loading=\"lazy\" />\n\n\u003Ch2>Jenis-Jenis Pass Box: Statis, Dinamis, dan UV\u003C/h2>\n\n\u003Cp>Secara umum, pass box untuk cleanroom terbagi dalam tiga kategori utama:\u003C/p>\n\n\u003Ch3>1. Pass Box Statis (Static Pass Box)\u003C/h3>\n\u003Cp>Pass box statis tidak memiliki sistem filtrasi udara aktif. Cocok untuk transfer antar ruangan dengan \u003Cstrong>klasifikasi ISO yang sama\u003C/strong> atau dari zona lebih bersih ke zona kurang bersih. Biaya lebih rendah dan perawatan minimal, namun tidak direkomendasikan untuk transfer dari area kotor ke area steril tanpa prosedur pembersihan manual. Pelajari perbedaannya secara detail di artikel \u003Ca href=\"/artikel/pass-box-statis-vs-dinamis-cleanroom-panduan-memilih\">pass box statis vs dinamis cleanroom\u003C/a>.\u003C/p>\n\n\u003Ch3>2. Pass Box Dinamis (Dynamic Pass Box)\u003C/h3>\n\u003Cp>Dilengkapi dengan \u003Cstrong>HEPA filter dan blower\u003C/strong> yang menyuplai udara bersih ke dalam chamber secara kontinu. Pass box dinamis wajib digunakan saat mentransfer material dari zona ISO lebih rendah ke zona ISO lebih tinggi (misalnya ISO 8 ke ISO 7). Udara tersaring HEPA menciptakan positive pressure yang mencegah partikel luar masuk.\u003C/p>\n\n\u003Ch3>3. Pass Box UV (UV Pass Box)\u003C/h3>\n\u003Cp>Dilengkapi lampu \u003Cstrong>UV-C germicidal (254 nm)\u003C/strong> untuk sterilisasi permukaan barang yang ditransfer. Sangat penting untuk fasilitas farmasi yang menangani bahan steril dan industri makanan yang memerlukan dekontaminasi kemasan. Durasi penyinaran UV biasanya 15-30 menit per siklus, dengan \u003Cem>interlock safety\u003C/em> yang mencegah pintu terbuka saat UV aktif.\u003C/p>\n\n\u003Ch2>Standar ISO 14644 dan GMP yang Harus Dipenuhi\u003C/h2>\n\n\u003Cp>Pass box untuk industri farmasi dan makanan harus memenuhi persyaratan ketat:\u003C/p>\n\n\u003Cul>\n  \u003Cli>\u003Cstrong>ISO 14644-1:2015\u003C/strong> — Klasifikasi kebersihan udara berdasarkan konsentrasi partikel. Pass box harus mampu mempertahankan klasifikasi ruangan di kedua sisi tanpa menambah kontaminasi.\u003C/li>\n  \u003Cli>\u003Cstrong>ISO 14644-3:2019\u003C/strong> — Metode pengujian cleanroom termasuk \u003Cem>filter leakage test\u003C/em> dan \u003Cem>airflow velocity test\u003C/em> untuk pass box dinamis.\u003C/li>\n  \u003Cli>\u003Cstrong>GMP Annex 1 (EU)\u003C/strong> — Mensyaratkan penggunaan pass box ber-interlock untuk fasilitas produksi steril, dengan validasi rutin terhadap efektivitas UV dan integritas filter.\u003C/li>\n  \u003Cli>\u003Cstrong>CPOB 2018 (BPOM)\u003C/strong> — Pedoman Cara Pembuatan Obat yang Baik di Indonesia mewajibkan sistem transfer material yang tervalidasi dan terdokumentasi.\u003C/li>\n\u003C/ul>\n\n\u003Cp>Pass box yang memenuhi standar ini harus memiliki sertifikasi material (material certificate), laporan uji kebocoran filter (DOP/PAO test), dan protokol validasi operasional.\u003C/p>\n\n\u003Ch2>Material Pass Box: Stainless Steel vs Pilihan Lain\u003C/h2>\n\n\u003Cp>Material konstruksi pass box sangat mempengaruhi durabilitas, kemudahan pembersihan, dan ketahanan terhadap bahan kimia pembersih:\u003C/p>\n\n\u003Ctable>\n  \u003Ctr>\u003Cth>Material\u003C/th>\u003Cth>Kelebihan\u003C/th>\u003Cth>Kekurangan\u003C/th>\u003Cth>Cocok Untuk\u003C/th>\u003C/tr>\n  \u003Ctr>\u003Ctd>\u003Cstrong>SS304\u003C/strong>\u003C/td>\u003Ctd>Tahan korosi, mudah dibersihkan, food-grade\u003C/td>\u003Ctd>Harga menengah\u003C/td>\u003Ctd>Cleanroom farmasi & makanan standar\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>\u003Cstrong>SS316L\u003C/strong>\u003C/td>\u003Ctd>Tahan asam & klorida, permukaan electropolished\u003C/td>\u003Ctd>Harga lebih tinggi\u003C/td>\u003Ctd>Farmasi steril, bahan kimia agresif\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>\u003Cstrong>Powder Coated Steel\u003C/strong>\u003C/td>\u003Ctd>Ekonomis\u003C/td>\u003Ctd>Rentan gores, tidak tahan desinfektan kuat\u003C/td>\u003Ctd>Hanya area non-kritis\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>\u003Cstrong>PVC/Plastik\u003C/strong>\u003C/td>\u003Ctd>Ringan, anti-static\u003C/td>\u003Ctd>Kurang rigid\u003C/td>\u003Ctd>Area ESD, industri elektronik\u003C/td>\u003C/tr>\n\u003C/table>\n\n\u003Cp>Untuk cleanroom farmasi dan makanan, \u003Cstrong>SS304 minimal\u003C/strong> — dan SS316L jika proses melibatkan disinfektan agresif seperti hydrogen peroxide vapor (HPV) atau chlorine-based sanitizer.\u003C/p>\n\n\u003Ch2>Ukuran Pass Box: Menyesuaikan dengan Kebutuhan Transfer\u003C/h2>\n\n\u003Cp>Ukuran pass box harus disesuaikan dengan dimensi material terbesar yang akan ditransfer. Dimensi standar pass box yang umum tersedia:\u003C/p>\n\n\u003Cul>\n  \u003Cli>\u003Cstrong>Kecil\u003C/strong>: 600 × 600 × 600 mm — untuk vial, ampul, sampel laboratorium\u003C/li>\n  \u003Cli>\u003Cstrong>Sedang\u003C/strong>: 800 × 800 × 800 mm — untuk wadah bahan baku, peralatan kecil\u003C/li>\n  \u003Cli>\u003Cstrong>Besar\u003C/strong>: 1000 × 1000 × 1000 mm ke atas — untuk drum, karton kemasan, peralatan produksi\u003C/li>\n  \u003Cli>\u003Cstrong>Custom\u003C/strong>: Dapat disesuaikan dengan kebutuhan spesifik layout cleanroom\u003C/li>\n\u003C/ul>\n\n\u003Cp>Aturan praktis: dimensi internal harus minimal \u003Cstrong>20% lebih besar\u003C/strong> dari barang terbesar yang akan dilewatkan untuk memudahkan bongkar muat tanpa menyentuh dinding chamber. Untuk kebutuhan logistik yang lebih besar, lihat panduan \u003Ca href=\"/artikel/pass-box-logistik-material-handling-cleanroom-2026\">pass box untuk logistik cleanroom\u003C/a>.\u003C/p>\n\n\u003Ch2>Fitur Interlock: Mencegah Kontaminasi Silang\u003C/h2>\n\n\u003Cp>Sistem interlock adalah mekanisme keamanan paling kritis pada pass box. Ada dua jenis:\u003C/p>\n\n\u003Cul>\n  \u003Cli>\u003Cstrong>Interlock Mekanis\u003C/strong>: Menggunakan kabel dan tuas — kedua pintu tidak dapat terbuka bersamaan secara fisik. Ekonomis tapi memerlukan perawatan berkala.\u003C/li>\n  \u003Cli>\u003Cstrong>Interlock Elektromagnetik\u003C/strong>: Menggunakan sensor dan solenoid lock. Kedua pintu terkunci secara elektronik; satu pintu hanya bisa dibuka jika pintu lainnya tertutup rapat. Lebih andal dan wajib untuk aplikasi farmasi steril.\u003C/li>\n\u003C/ul>\n\n\u003Cp>Fitur tambahan yang penting: \u003Cstrong>indikator status pintu\u003C/strong> (LED merah/hijau), \u003Cstrong>timer UV otomatis\u003C/strong>, dan \u003Cstrong>emergency release\u003C/strong> untuk situasi darurat. Pastikan interlock telah diuji sesuai standar IEC 61508 untuk safety integrity.\u003C/p>\n\n\u003Ch2>Perbandingan Kebutuhan Pass Box: Farmasi vs Industri Makanan\u003C/h2>\n\n\u003Cp>Tidak semua pass box cocok untuk semua industri. Berikut perbandingan kebutuhan spesifik:\u003C/p>\n\n\u003Ctable>\n  \u003Ctr>\u003Cth>Aspek\u003C/th>\u003Cth>Farmasi\u003C/th>\u003Cth>Makanan\u003C/th>\u003C/tr>\n  \u003Ctr>\u003Ctd>Klasifikasi Cleanroom\u003C/td>\u003Ctd>ISO 5-8 (Grade A-D)\u003C/td>\u003Ctd>ISO 7-8 umumnya\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>Jenis Pass Box\u003C/td>\u003Ctd>Dinamis + UV (wajib untuk steril)\u003C/td>\u003Ctd>Statis dengan UV (cukup untuk mayoritas kasus)\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>Material\u003C/td>\u003Ctd>SS316L electropolished\u003C/td>\u003Ctd>SS304 food-grade\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>Validasi\u003C/td>\u003Ctd>IQ/OQ/PQ lengkap, DOP test\u003C/td>\u003Ctd>Validasi pembersihan, swab test\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>Sertifikasi\u003C/td>\u003Ctd>BPOM CPOB, EU GMP Annex 1\u003C/td>\u003Ctd>HACCP, ISO 22000\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>Frekuensi UV\u003C/td>\u003Ctd>Setiap siklus transfer\u003C/td>\u003Ctd>Setiap batch atau per shift\u003C/td>\u003C/tr>\n\u003C/table>\n\n\u003Ch2>Checklist: 7 Hal yang Harus Dicek Sebelum Membeli Pass Box\u003C/h2>\n\n\u003Col>\n  \u003Cli>\u003Cstrong>Klasifikasi cleanroom target\u003C/strong> — Tentukan ISO class di kedua sisi pass box. Jika ada perbedaan >1 level, wajib dynamic pass box.\u003C/li>\n  \u003Cli>\u003Cstrong>Dimensi material transfer\u003C/strong> — Ukur dimensi maksimum barang yang akan dipindahkan; tambahkan margin 20%.\u003C/li>\n  \u003Cli>\u003Cstrong>Jenis material konstruksi\u003C/strong> — Pastikan sesuai dengan chemical resistance yang dibutuhkan terhadap desinfektan yang digunakan.\u003C/li>\n  \u003Cli>\u003Cstrong>Sistem interlock\u003C/strong> — Elektromagnetik untuk aplikasi kritis; verifikasi sertifikasi safety.\u003C/li>\n  \u003Cli>\u003Cstrong>Filtrasi\u003C/strong> — HEPA H13 minimum untuk dynamic pass box; cek availability filter pengganti di Indonesia.\u003C/li>\n  \u003Cli>\u003Cstrong>Lampu UV\u003C/strong> — Jika diperlukan, pastikan intensitas UV ≥ 200 μW/cm² dan dilengkapi hour-meter untuk jadwal penggantian.\u003C/li>\n  \u003Cli>\u003Cstrong>Dokumentasi dan after-sales\u003C/strong> — Pastikan supplier menyediakan FAT/SAT protocol, manual instalasi, dan dukungan teknis di Indonesia.\u003C/li>\n\u003C/ol>\n\n\u003Ch2>Kesalahan Umum dalam Memilih Pass Box dan Cara Menghindarinya\u003C/h2>\n\n\u003Cp>Berdasarkan pengalaman proyek cleanroom di Indonesia, berikut kesalahan yang paling sering terjadi:\u003C/p>\n\n\u003Cul>\n  \u003Cli>\u003Cstrong>Memilih pass box statis untuk zona berbeda level\u003C/strong> — Akibat: kegagalan validasi ISO. Solusi: selalu evaluasi pressure cascade cleanroom sebelum menentukan tipe.\u003C/li>\n  \u003Cli>\u003Cstrong>Mengabaikan material interior\u003C/strong> — Permukaan kasar menjadi tempat akumulasi partikel. Pastikan Ra ≤ 0.8 μm untuk aplikasi farmasi.\u003C/li>\n  \u003Cli>\u003Cstrong>Tidak mempertimbangkan ekspansi\u003C/strong> — Beli pass box yang terlalu kecil. Beli dengan margin kapasitas 30% untuk antisipasi peningkatan produksi.\u003C/li>\n  \u003Cli>\u003Cstrong>Melewatkan FAT (Factory Acceptance Test)\u003C/strong> — Selalu minta FAT report sebelum pengiriman, termasuk uji kebocoran filter dan fungsi interlock.\u003C/li>\n  \u003Cli>\u003Cstrong>Tidak ada protokol pembersihan\u003C/strong> — Pass box harus masuk jadwal pembersihan rutin cleanroom; dokumentasikan frekuensi dan metode pembersihan.\u003C/li>\n\u003C/ul>\n\n\u003Ch2>FAQ: Pertanyaan Umum tentang Pass Box Cleanroom\u003C/h2>\n\n\u003Ch3>Apa perbedaan pass box statis dan dinamis untuk cleanroom farmasi?\u003C/h3>\n\u003Cp>Pass box statis tidak memiliki sistem filtrasi aktif dan cocok untuk antar zona ISO yang sama. Pass box dinamis dilengkapi HEPA filter dan blower, wajib digunakan saat mentransfer material dari ISO lebih rendah ke ISO lebih tinggi. Untuk farmasi steril, pass box dinamis adalah standar minimum yang diwajibkan oleh CPOB dan EU GMP Annex 1.\u003C/p>\n\n\u003Ch3>Apakah pass box wajib memiliki lampu UV?\u003C/h3>\n\u003Cp>Tidak selalu wajib. Lampu UV diperlukan jika Anda mentransfer material yang memerlukan dekontaminasi permukaan, seperti kemasan primer obat steril atau bahan baku makanan siap konsumsi. Untuk aplikasi non-steril, pass box tanpa UV dapat digunakan selama prosedur pembersihan manual diterapkan secara konsisten.\u003C/p>\n\n\u003Ch3>Berapa ukuran pass box yang ideal untuk industri makanan?\u003C/h3>\n\u003Cp>Untuk industri makanan skala menengah, ukuran 800 × 800 × 800 mm umumnya mencukupi untuk transfer bahan baku dalam wadah standar. Namun, jika Anda memindahkan drum atau karton besar, pertimbangkan ukuran 1000 × 1000 × 1000 mm atau custom. Selalu tambahkan margin 20% dari dimensi barang terbesar.\u003C/p>\n\n\u003Ch3>Bagaimana cara memastikan pass box memenuhi standar GMP?\u003C/h3>\n\u003Cp>Pastikan pass box memiliki: (1) material sertifikat untuk SS304/316L, (2) laporan DOP/PAO test untuk integritas HEPA filter (jika dinamis), (3) sistem interlock yang tervalidasi, (4) protokol IQ/OQ/PQ yang lengkap, dan (5) surface roughness ≤ 0.8 μm Ra untuk aplikasi farmasi. Minta dokumentasi ini dari supplier sebelum pembelian.\u003C/p>","\u003Ch2>什么是传递窗？为什么它对制药和食品洁净室如此重要？\u003C/h2>\n\n\u003Cp>传递窗（Pass Box），也称为\u003Cem>通过式传递舱\u003C/em>或\u003Cem>转运舱口\u003C/em>，是一种用于洁净室区域之间物料转移的装置，旨在最大限度地减少交叉污染。对于必须遵守\u003Cstrong>ISO 14644\u003C/strong>和\u003Cstrong>GMP（良好生产规范）\u003C/strong>标准的制药和食品行业设施来说，它是关键的组成部分。\u003C/p>\n\n\u003Cp>在制药洁净室中，不同洁净级别区域之间（例如从ISO 8级到ISO 7级）的每一次原料、检测样品或生产设备的转移都必须通过传递窗进行。没有合适的传递窗，直接开启房间之间的门会导致颗粒数量激增和BPOM审计失败。\u003C/p>\n\n\u003Cp>对于食品行业，传递窗在将物料从准备区转移到无菌包装区时，能够有效防止微生物污染。\u003Cstrong>FDA食品安全现代化法案\u003C/strong>的数据显示，23%的食品产品召回与物料转移过程中的污染控制失败有关。\u003C/p>\n\n\u003Cp>选择合适的传递窗不仅仅是购买一个不锈钢箱子——技术规格必须与您的洁净室级别、所转移的物料以及使用频率相匹配。另请参阅我们关于\u003Ca href=\"/artikel/bahan-dinding-cleanroom-panduan-lengkap\">洁净室墙体材料\u003C/a>的综合指南，全面了解洁净室设备生态系统。\u003C/p>\n\n\u003Cimg src=\"https://assets.sandwichpanels.id/blog/1783058576170-20260703-060256-pass-box-dinamis-diagram-01.jpg\" alt=\"动态传递窗示意图，含HEPA过滤器和洁净室区域之间的气流\" loading=\"lazy\" />\n\n\u003Ch2>传递窗的类型：静态、动态和紫外线\u003C/h2>\n\n\u003Cp>一般来说，洁净室传递窗可分为三大类：\u003C/p>\n\n\u003Ch3>1. 静态传递窗（Static Pass Box）\u003C/h3>\n\u003Cp>静态传递窗没有主动空气过滤系统。适用于\u003Cstrong>相同ISO级别\u003C/strong>的房间之间，或从较洁净区域到次洁净区域的转移。成本较低，维护量小，但不建议用于从污染区域到无菌区域的转移，除非配合手动清洁程序。详细了解差异，请参阅我们关于\u003Ca href=\"/artikel/pass-box-statis-vs-dinamis-cleanroom-panduan-memilih\">静态与动态传递窗\u003C/a>的文章。\u003C/p>\n\n\u003Ch3>2. 动态传递窗（Dynamic Pass Box）\u003C/h3>\n\u003Cp>配备\u003Cstrong>HEPA过滤器和风机\u003C/strong>，持续向舱内供应洁净空气。当将物料从较低ISO级别区域转移到较高级别区域（例如从ISO 8到ISO 7）时，动态传递窗是强制要求。经过HEPA过滤的空气产生正压，阻止外部颗粒进入。\u003C/p>\n\n\u003Ch3>3. 紫外线传递窗（UV Pass Box）\u003C/h3>\n\u003Cp>配备\u003Cstrong>UV-C杀菌灯（254 nm）\u003C/strong>，用于对转移物品进行表面灭菌。对于处理无菌物料的制药设施和需要包装净化的食品行业至关重要。紫外线照射通常每周期持续15-30分钟，并配备\u003Cem>互锁安全\u003C/em>功能，防止UV工作时门被打开。\u003C/p>\n\n\u003Ch2>必须满足的ISO 14644和GMP标准\u003C/h2>\n\n\u003Cp>制药和食品行业使用的传递窗必须满足严格的要求：\u003C/p>\n\n\u003Cul>\n  \u003Cli>\u003Cstrong>ISO 14644-1:2015\u003C/strong> — 基于颗粒浓度的空气洁净度分级。传递窗必须保持两侧房间的级别，而不增加污染。\u003C/li>\n  \u003Cli>\u003Cstrong>ISO 14644-3:2019\u003C/strong> — 洁净室测试方法，包括动态传递窗的\u003Cem>过滤器泄漏测试\u003C/em>和\u003Cem>气流速度测试\u003C/em>。\u003C/li>\n  \u003Cli>\u003Cstrong>GMP附录1（欧盟）\u003C/strong> — 要求无菌生产设施使用带互锁的传递窗，并对UV效果和过滤器完整性进行常规验证。\u003C/li>\n  \u003Cli>\u003Cstrong>CPOB 2018（印度尼西亚BPOM）\u003C/strong> — 印度尼西亚的良好生产规范指南，要求经过验证和记录的物料转移系统。\u003C/li>\n\u003C/ul>\n\n\u003Cp>符合标准的传递窗应附带材料证书、过滤器泄漏测试报告（DOP/PAO测试）和操作验证方案。\u003C/p>\n\n\u003Ch2>传递窗材料：不锈钢与其他选择\u003C/h2>\n\n\u003Cp>传递窗的结构材料显著影响耐久性、可清洁性以及对清洁化学品的耐受性：\u003C/p>\n\n\u003Ctable>\n  \u003Ctr>\u003Cth>材料\u003C/th>\u003Cth>优点\u003C/th>\u003Cth>缺点\u003C/th>\u003Cth>适用场景\u003C/th>\u003C/tr>\n  \u003Ctr>\u003Ctd>\u003Cstrong>SS304\u003C/strong>\u003C/td>\u003Ctd>耐腐蚀、易清洁、食品级\u003C/td>\u003Ctd>中档成本\u003C/td>\u003Ctd>标准制药与食品洁净室\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>\u003Cstrong>SS316L\u003C/strong>\u003C/td>\u003Ctd>耐酸碱氯化物、电解抛光表面\u003C/td>\u003Ctd>成本较高\u003C/td>\u003Ctd>无菌制药、强化学品环境\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>\u003Cstrong>粉末涂层钢\u003C/strong>\u003C/td>\u003Ctd>经济实惠\u003C/td>\u003Ctd>易刮伤、不耐受强消毒剂\u003C/td>\u003Ctd>仅限非关键区域\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>\u003Cstrong>PVC/塑料\u003C/strong>\u003C/td>\u003Ctd>轻便、防静电\u003C/td>\u003Ctd>刚性较差\u003C/td>\u003Ctd>ESD区域、电子行业\u003C/td>\u003C/tr>\n\u003C/table>\n\n\u003Cp>对于制药和食品洁净室，\u003Cstrong>至少使用SS304\u003C/strong>——如果工艺涉及过氧化氢蒸汽（HPV）或含氯消毒剂等强化学品，则应使用SS316L。\u003C/p>\n\n\u003Ch2>传递窗尺寸：匹配您的转移需求\u003C/h2>\n\n\u003Cp>传递窗的尺寸应与需要转移的最大物品相匹配。常见的标准尺寸包括：\u003C/p>\n\n\u003Cul>\n  \u003Cli>\u003Cstrong>小型\u003C/strong>：600 × 600 × 600 mm — 适用于小瓶、安瓿瓶、实验室样品\u003C/li>\n  \u003Cli>\u003Cstrong>中型\u003C/strong>：800 × 800 × 800 mm — 适用于原料容器、小型设备\u003C/li>\n  \u003Cli>\u003Cstrong>大型\u003C/strong>：1000 × 1000 × 1000 mm及以上 — 适用于桶、包装纸箱、生产设备\u003C/li>\n  \u003Cli>\u003Cstrong>定制\u003C/strong>：根据具体洁净室布局要求定制\u003C/li>\n\u003C/ul>\n\n\u003Cp>经验法则：内部尺寸应至少比要通过的最大物品\u003Cstrong>大20%\u003C/strong>，以便轻松装卸而不触碰舱壁。对于更大的物流需求，请参阅我们的\u003Ca href=\"/artikel/pass-box-logistik-material-handling-cleanroom-2026\">洁净室传递窗物流指南\u003C/a>。\u003C/p>\n\n\u003Ch2>互锁功能：防止交叉污染\u003C/h2>\n\n\u003Cp>互锁系统是传递窗上最关键的安全机制。有两种类型：\u003C/p>\n\n\u003Cul>\n  \u003Cli>\u003Cstrong>机械互锁\u003C/strong>：使用线缆和杠杆——两扇门在物理上无法同时打开。经济实惠，但需要定期维护。\u003C/li>\n  \u003Cli>\u003Cstrong>电磁互锁\u003C/strong>：使用传感器和电磁锁。两扇门均通过电子方式锁定；只有当另一扇门完全关闭时，才能打开当前门。更可靠，是无菌制药应用的强制要求。\u003C/li>\n\u003C/ul>\n\n\u003Cp>重要的附加功能：\u003Cstrong>门状态指示灯\u003C/strong>（红色/绿色LED）、\u003Cstrong>自动UV计时器\u003C/strong>和\u003Cstrong>紧急释放装置\u003C/strong>。确保互锁已按照IEC 61508安全完整性标准进行测试。\u003C/p>\n\n\u003Ch2>传递窗需求对比：制药与食品行业\u003C/h2>\n\n\u003Cp>并非所有传递窗都适用于每个行业。以下是具体需求的对比：\u003C/p>\n\n\u003Ctable>\n  \u003Ctr>\u003Cth>方面\u003C/th>\u003Cth>制药\u003C/th>\u003Cth>食品\u003C/th>\u003C/tr>\n  \u003Ctr>\u003Ctd>洁净室分级\u003C/td>\u003Ctd>ISO 5-8（A-D级）\u003C/td>\u003Ctd>通常ISO 7-8\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>传递窗类型\u003C/td>\u003Ctd>动态+UV（无菌强制要求）\u003C/td>\u003Ctd>静态带UV（大多数情况足够）\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>材料\u003C/td>\u003Ctd>SS316L电解抛光\u003C/td>\u003Ctd>SS304食品级\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>验证\u003C/td>\u003Ctd>完整的IQ/OQ/PQ、DOP测试\u003C/td>\u003Ctd>清洁验证、拭子测试\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>认证\u003C/td>\u003Ctd>BPOM CPOB、EU GMP附录1\u003C/td>\u003Ctd>HACCP、ISO 22000\u003C/td>\u003C/tr>\n  \u003Ctr>\u003Ctd>UV频率\u003C/td>\u003Ctd>每次转移周期\u003C/td>\u003Ctd>每批次或每班次\u003C/td>\u003C/tr>\n\u003C/table>\n\n\u003Ch2>检查清单：购买传递窗前必须核对的7个要点\u003C/h2>\n\n\u003Col>\n  \u003Cli>\u003Cstrong>目标洁净室级别\u003C/strong> — 确定传递窗两侧的ISO级别。如果级别差异超过1级，必须使用动态传递窗。\u003C/li>\n  \u003Cli>\u003Cstrong>转移物料尺寸\u003C/strong> — 测量需要转移物品的最大尺寸；增加20%的余量。\u003C/li>\n  \u003Cli>\u003Cstrong>结构材料类型\u003C/strong> — 确保与您使用的消毒剂所需的化学耐受性相匹配。\u003C/li>\n  \u003Cli>\u003Cstrong>互锁系统\u003C/strong> — 关键应用使用电磁互锁；验证安全认证。\u003C/li>\n  \u003Cli>\u003Cstrong>过滤\u003C/strong> — 动态传递窗至少需要HEPA H13级别；检查本地替换过滤器的供应情况。\u003C/li>\n  \u003Cli>\u003Cstrong>紫外线灯\u003C/strong> — 如需要，确保UV强度≥200 μW/cm²，并配备计时器以便按计划更换。\u003C/li>\n  \u003Cli>\u003Cstrong>文件和售后服务\u003C/strong> — 确保供应商提供FAT/SAT方案、安装手册和本地技术支持。\u003C/li>\n\u003C/ol>\n\n\u003Ch2>选择传递窗的常见错误及如何避免\u003C/h2>\n\n\u003Cp>基于印度尼西亚洁净室项目经验，以下是常见的错误：\u003C/p>\n\n\u003Cul>\n  \u003Cli>\u003Cstrong>为不同级别区域选择静态传递窗\u003C/strong> — 后果：ISO验证失败。解决方案：在选择类型前，始终评估洁净室压力梯度。\u003C/li>\n  \u003Cli>\u003Cstrong>忽视内部材料表面处理\u003C/strong> — 粗糙表面会成为颗粒积聚点。制药应用应确保Ra ≤ 0.8 μm。\u003C/li>\n  \u003Cli>\u003Cstrong>未考虑扩展需求\u003C/strong> — 购买的传递窗太小。应以30%的容量余量购买，以应对生产增长。\u003C/li>\n  \u003Cli>\u003Cstrong>跳过FAT（出厂验收测试）\u003C/strong> — 发货前始终要求FAT报告，包括过滤器泄漏测试和互锁功能测试。\u003C/li>\n  \u003Cli>\u003Cstrong>缺少清洁规程\u003C/strong> — 传递窗必须纳入洁净室的日常清洁计划中；记录清洁频率和方法。\u003C/li>\n\u003C/ul>\n\n\u003Ch2>常见问题：洁净室传递窗问答\u003C/h2>\n\n\u003Ch3>制药洁净室的静态和动态传递窗有什么区别？\u003C/h3>\n\u003Cp>静态传递窗没有主动过滤系统，适用于相同ISO级别的区域之间。动态传递窗配备HEPA过滤器和风机，当从较低ISO级别区域向较高级别区域转移物料时是强制要求。对于无菌药品生产，动态传递窗是CPOB和EU GMP附录1要求的最低标准。\u003C/p>\n\n\u003Ch3>洁净室传递窗必须配备紫外线灯吗？\u003C/h3>\n\u003Cp>并非总是必须。紫外线灯在需要表面净化的物料转移中是必需的，例如无菌药品初级包装或即食食品原料。对于非无菌应用，只要始终执行手动清洁程序，即可使用不带UV的传递窗。\u003C/p>\n\n\u003Ch3>食品行业理想的传递窗尺寸是多少？\u003C/h3>\n\u003Cp>对于中等规模的食品加工，800 × 800 × 800 mm的尺寸通常足以使用标准容器转移原料。但是，如果您需要转移桶或大纸箱，请考虑1000 × 1000 × 1000 mm或定制尺寸。始终在最大物品尺寸上增加20%的余量。\u003C/p>\n\n\u003Ch3>如何确保传递窗符合GMP标准？\u003C/h3>\n\u003Cp>确保传递窗具备：(1) SS304/316L材料证书，(2) HEPA过滤器完整性的DOP/PAO测试报告（如果是动态的），(3) 经过验证的互锁系统，(4) 完整的IQ/OQ/PQ方案，以及(5) 制药应用表面粗糙度Ra ≤ 0.8 μm。购买前请向供应商索取这些文件。\u003C/p>","https://assets.sandwichpanels.id/blog/1783058484150-20260703-060123-pass-box-cleanroom-01.jpg","2026-07-17T02:25:05.908469Z",{"en":248,"id":249,"zh":250},"What Is a Pass Box and Why It Matters for Pharma & Food Cleanrooms\n\nA pass box — also known as a pass-through chamber or transfer hatch — is a material transfer device between cleanroom zones, des...","Apa Itu Pass Box dan Mengapa Penting untuk Cleanroom Farmasi & Makanan?\n\nPass box — juga dikenal sebagai pass-through chamber atau transfer hatch — adalah perangkat pemindah material antar ruangan...","什么是传递窗？为什么它对制药和食品洁净室如此重要？\n\n传递窗（Pass Box），也称为通过式传递舱或转运舱口，是一种用于洁净室区域之间物料转移的�...","b6d94297-8e62-451f-8f20-5b3d78568f6a",true,"2026-07-17T02:25:05.904014Z",{"title":255,"description":259},{"en":256,"id":257,"zh":258},"How to Choose Pass Box for Pharma & Food Cleanrooms: ISO-GMP Guide","Cara Memilih Pass Box Cleanroom Farmasi & Makanan: Panduan ISO-GMP","制药食品洁净室传递窗选购指南：ISO-GMP",{"en":260,"id":261,"zh":262},"How to choose the right pass box for pharma and food cleanrooms based on ISO 14644 and GMP standards. Types, materials, sizing, UV and interlock features explained.","Panduan memilih pass box untuk cleanroom farmasi dan makanan berdasarkan standar ISO 14644 dan GMP. Pelajari jenis, material, ukuran, dan fitur UV/interlock.","基于ISO 14644和GMP标准，为制药和食品洁净室选择合适的传递窗。类型、材料、尺寸、紫外线和互锁功能详解。","cara-memilih-pass-box-cleanroom-farmasi-makanan-2026",[265,69,266,267,268,269,270,271],"pass box","farmasi","makanan","ISO","GMP","cara memilih","peralatan cleanroom",{"en":256,"id":257,"zh":258},{"data":274,"total":408},[275,304,328,352,380],{"author_name":238,"category":276,"cover_image":282,"created_at":283,"excerpt":284,"id":288,"published_at":289,"slug":290,"tags":291,"title":299,"updated_at":303},{"name":277,"slug":281},{"en":278,"id":279,"zh":280},"Industry & Applications","Industri & Aplikasi","行业与应用","industri","https://assets.sandwichpanels.id/blog/1786652012493-sandwich-panel-data-center-konstruksi-modular-2026.png","2026-08-12T20:28:58.745519Z",{"en":285,"id":286,"zh":287},"Installed data center capacity in Indonesia reached roughly 520 MW by June 2026. IDPRO chairman Hendra Suryakusuma expects the national figure to approach 600 MW by year end, driven by projects now en...","Kapasitas fasilitas data center di Indonesia menyentuh sekitar 520 MW sampai Juni 2026. Ketua Umum IDPRO Hendra Suryakusuma memperkirakan angka itu bisa mendekati 600 MW di penghujung tahun, ditopang ...","截至2026年6月，印尼已建成的数据中心容量约为520兆瓦。印尼数据中心产业协会（IDPRO）主席Hendra Suryakusuma预计，随着多个项目进入施工、通电与调试阶�...","80e08120-6448-4e7e-a60a-585a70c450b2","2026-08-13T02:18:40.179129Z","sandwich-panel-data-center-konstruksi-modular-2026",[292,293,294,295,296,297,298],"sandwich panel data center","konstruksi data center indonesia","NFPA 75","TIA-942","ASHRAE TC 9.9","panel rockwool tahan api","modular data center",{"en":300,"id":301,"zh":302},"Sandwich Panels for Data Centers: Fire-Rated Build 2026","Sandwich Panel Data Center: Konstruksi Modular Tahan Api 2026","数据中心夹芯板：模块化防火建造指南2026","2026-08-13T20:13:36.359217Z",{"author_name":238,"category":305,"cover_image":307,"created_at":308,"excerpt":309,"id":313,"published_at":314,"slug":315,"tags":316,"title":324,"updated_at":314},{"name":306,"slug":281},{"en":278,"id":279,"zh":280},"https://assets.sandwichpanels.id/blog/1786479336522-sandwich-panel-cold-storage-container-mobile-cold-room-cover-01.png","2026-08-11T20:21:41.478687Z",{"en":310,"id":311,"zh":312},"Fishermen along Java's northern coast routinely hold their catch for hours before a collector's truck arrives. Horticulture growers face the same squeeze. Permanent cold storage sits too far from the ...","Nelayan di pantai utara Jawa sering menahan hasil tangkapan berjam-jam sebelum truk pengepul datang. Petani hortikultura menghadapi persoalan serupa. Cold storage permanen terlalu jauh dari titik pane...","爪哇北岸的渔民常常要等上几个小时，收购车才会抵达码头。园艺种植户面临同样的困境：固定式冷库离产地太远、容量过大、投资回报算不过来。集��...","8c116a8f-bd98-415c-96e2-1b00d7a7240b","2026-08-12T03:05:12.276049Z","sandwich-panel-cold-storage-container-mobile-cold-room-2026",[317,318,319,320,321,322,323],"cold storage container","mobile cold room","cold room portable","sandwich panel PIR","ketebalan panel cold storage","rantai dingin perikanan","reefer container",{"en":325,"id":326,"zh":327},"Container Cold Storage & Mobile Cold Rooms Guide 2026","Cold Storage Container & Mobile Cold Room Panel 2026","集装箱冷库与移动冷藏室：夹芯板选型指南2026",{"author_name":238,"category":329,"cover_image":331,"created_at":332,"excerpt":333,"id":337,"published_at":338,"slug":339,"tags":340,"title":348,"updated_at":338},{"name":330,"slug":281},{"en":278,"id":279,"zh":280},"https://assets.sandwichpanels.id/blog/1786393070543-sandwich-panel-pabrik-baterai-ev-dry-room-cover-01.png","2026-08-10T20:21:34.205599Z",{"en":334,"id":335,"zh":336},"Indonesia's electric vehicle (EV) battery industry has entered a new phase. The battery plant of PT CATL Amperex Technology Indonesia Battery (CATIB), a joint venture between Contemporary Amperex Tech...","Industri baterai kendaraan listrik (EV) Indonesia memasuki babak baru. Pabrik baterai PT CATL Amperex Technology Indonesia Battery (CATIB), hasil kerja sama Contemporary Amperex Technology Co. Limited...","印度尼西亚电动汽车（EV）电池产业迈入新阶段。由宁德时代（CATL）子公司CBL与印尼电池公司（IBC）合资的PT CATL Amperex Technology Indonesia Battery（CATIB）电�...","460950c8-6e0f-44af-8b1f-707d02338c6d","2026-08-11T02:16:05.725517Z","sandwich-panel-pabrik-baterai-ev-dry-room-2026",[341,342,343,344,345,346,347],"sandwich panel pabrik baterai ev","dry room baterai","PIR sandwich panel","fire rating EI60 EI120","cleanroom industri","CATL Karawang","konstruksi pabrik baterai",{"en":349,"id":350,"zh":351},"Sandwich Panels for EV Battery Plants & Dry Rooms 2026","Sandwich Panel Pabrik Baterai EV & Dry Room 2026","EV电池工厂与干燥室夹芯板建造指南2026",{"author_name":238,"category":353,"cover_image":359,"created_at":360,"excerpt":361,"id":365,"published_at":366,"slug":367,"tags":368,"title":376,"updated_at":366},{"name":354,"slug":358},{"en":355,"id":356,"zh":357},"Product Comparisons","Perbandingan Produk","产品比较","perbandingan","https://assets.sandwichpanels.id/blog/1786306267791-sandwich-panel-vs-acp-aluminium-composite-panel-cover-01.png","2026-08-09T20:15:18.683434Z",{"en":362,"id":363,"zh":364},"Many buyers assume ACP (Aluminium Composite Panel) and sandwich panel are the same product because both get installed as an exterior wall layer. In reality they are fundamentally different: ACP is a d...","Banyak calon pembeli mengira ACP (Aluminium Composite Panel) dan sandwich panel adalah produk yang sama karena sama-sama dipasang sebagai lapisan dinding luar bangunan. Padahal keduanya berbeda secara...","很多客户以为ACP铝塑板和夹芯板是同一种材料，因为两者都安装在建筑外墙表面。实际上二者本质完全不同：ACP是一种纯装饰性幕墙材料，不具备结构��...","0736e4bc-30e8-4003-a07c-c6be28c7a400","2026-08-10T02:16:32.442421Z","sandwich-panel-vs-acp-perbedaan-dan-cara-memilih-2026",[369,370,371,372,373,374,375],"sandwich panel vs acp","aluminium composite panel","perbandingan material fasad","EN 14509","SNI 1741","fire rating panel","material dinding pabrik",{"en":377,"id":378,"zh":379},"Sandwich Panel vs ACP: Key Differences & How to Choose 2026","Sandwich Panel vs ACP: Perbedaan dan Cara Memilih 2026","夹芯板与ACP铝塑板：区别与选购指南2026",{"author_name":238,"category":381,"cover_image":387,"created_at":388,"excerpt":389,"id":393,"published_at":394,"slug":395,"tags":396,"title":404,"updated_at":394},{"name":382,"slug":386},{"en":383,"id":384,"zh":385},"Guides & Tutorials","Panduan & Tutorial","指南与教程","panduan","https://assets.sandwichpanels.id/blog/1786219846540-bahan-dinding-cleanroom-panduan-pemilihan-sandwich-panel-2026-cover-01.png","2026-08-08T20:16:05.976199Z",{"en":390,"id":391,"zh":392},"Choosing the wrong cleanroom wall material is never just a cosmetic mistake. A panel with the wrong specification can trigger excess particle shedding, become hard to clean, or fail a GMP/CPOB audit o...","Kesalahan memilih bahan dinding cleanroom bukan sekadar soal estetika. Panel yang salah spesifikasi bisa memicu partikulasi berlebih, sulit dibersihkan, atau bahkan gagal audit CPOB/GMP saat inspeksi ...","洁净室墙面材料选错绝不只是外观问题。规格不当的夹芯板会导致颗粒物脱落超标、难以清洁,甚至在BPOM的CPOB审计中直接不合格。本文从技术角度讲解��...","611ca269-0aec-4a7a-843f-3e0d93d6a6c4","2026-08-09T02:16:22.637543Z","bahan-dinding-cleanroom-panduan-pemilihan-sandwich-panel-2026",[397,398,399,400,401,402,403],"bahan dinding cleanroom","kualifikasi cleanroom","sandwich panel cleanroom","ISO 14644","CPOB BPOM","core PU PIR rockwool","hairline joint cleanroom",{"en":405,"id":406,"zh":407},"Cleanroom Wall Materials: Sandwich Panel Selection Guide 2026","Bahan Dinding Cleanroom: Panduan Pemilihan Sandwich Panel 2026","洁净室墙面材料：夹芯板选型指南2026",175]