GMP & ISO 14644 Certified
PT. Far Clean Indonesia Cleanroom
Pilih Bahasa / Language:
Produsen Pass Box Dinamis Kustom untuk Cleanroom GMP Grade A – PT Far Clean Indonesia
GMP Kelas A Dinamis
Reduksi Mikroba 6-Log & Validasi Lampiran 1 GMP

Dirancang khusus untuk fasilitas steril farmasi dan bioteknologi dengan reduksi mikroba 6-log terbukti dan kepatuhan FDA 21 CFR Part 11.

Peralatan Steril Cleanroom ID: fc-passbox-dynamic

Produsen Dynamic Pass Box Kustom untuk Cleanroom GMP Grade A

Ruang Transfer Material Aseptik Tingkat Lanjut dengan HEPA H14 & Pengurangan Mikroba 6-Log

Farclean adalah produsen dynamic pass box khusus yang tepercaya, memberikan solusi transfer aseptik canggih untuk cleanroom farmasi, biologika, dan ilmu hayati GMP Grade A.

Rekomendasi Aplikasi Industri:

Suite Pengisian Aseptik GMP Grade A Manufaktur Biologika & Vaksin Bahan Farmasi Aktif (API) Laboratorium Kontainmen BSL-3/BSL-4 Kemasan Steril Alat Kesehatan

Keunggulan & Fitur Utama:

  • ✓ Mekanisme Geser Elektrik: Sistem pintu otomatis berbasis servo piston untuk operasi bebas sentuhan (hands-free).
  • ✓ Pengurangan Mikroba 6 - Log: Terbukti membasmi spora Bacillus atrophaeus sesuai standar ISO 14644-4 dan EU GMP Annex 1.
  • ✓ Siklus Urutan Terprogram: Siklus otomatisasi Dehumidifikasi, Sterilisasi, Pemindahan, dan Pembuangan terkontrol PLC.
  • ✓ Filtrasi Katalitik Tingkat Lanjut: Sistem filtrasi katalitik bawaan mengurai residu zat sterilisasi demi keselamatan operator.

* Kustomisasi dimensi ruang (chamber), opsi material SUS304 / SUS316L electropolish, integrasi port dan konektivitas BMS / SCADA.

Solusi Transfer Aseptik cGMP Grade A

Produsen Dynamic Pass Box Kustom untuk Cleanroom GMP Grade A

Lingkungan cleanroom GMP Kelas A memerlukan tindakan sterilisasi permukaan yang tepat sebelum produk biologis, bahan aktif farmasi, atau barang sensitif lainnya memasuki jalur produksi. Sebagai produsen dynamic pass box khusus yang terspesialisasi, Farclean merancang dan membangun enclosure transfer otomatis untuk reduksi mikroba total dan integrasi tanpa batas dengan infrastruktur cleanroom Anda termasuk pintu cleanroom yang tervalidasi dan panel dinding modular yang presisi.

Produsen Pass Box Dinamis Kustom untuk Cleanroom GMP Grade A – PT Far Clean Indonesia

Desain dan Pengoperasian Ruang Transfer yang Inovatif

Dynamic pass box Farclean dilengkapi teknologi sterilisasi mutakhir dan solusi kontainmen serbaguna yang disesuaikan dengan standar pengendalian kontaminasi paling ketat, memastikan produk Anda tetap terjaga integritasnya selama pemindahan:

01

Mekanisme Geser Elektrik

Sistem pintu berpenggerak piston kami yang telah dipatenkan memungkinkan pengoperasian sepenuhnya tanpa menggunakan tangan, menghilangkan sentuhan manusia dan potensi kontaminasi silang pada fasilitas yang sangat sensitif yang membutuhkan keselamatan hayati.

02

Integrasi Panel Dinding Modular

Tersedia sebagai unit berdiri bebas atau dirancang untuk terintegrasi mulus dengan sistem dinding cleanroom, memungkinkan konfigurasi optimal untuk protokol penanganan produk.

03

Siklus Urutan Terprogram

Siklus otomatisasi kustom mengelola secara presisi fase Dehumidifikasi, Sterilisasi, Pemindahan, dan Pembuangan untuk transfer dengan bioburden nol atau rendah antar lingkungan cleanroom yang berbeda.

04

Filtrasi Katalitik Tingkat Lanjut

Sistem filter terintegrasi mengurai sisa bahan sterilisasi, memastikan keselamatan menyeluruh dan kepatuhan terhadap regulasi lingkungan di fasilitas GMP.

05

Opsi Keranjang

Tersedia dengan penahan material steril yang dapat diganti dan dirancang untuk integrasi jangka panjang dengan panel dinding cleanroom kami yang tahan lama.

Metrik Kinerja Dynamic Pass Box

Parameter Sistem Spesifikasi Teknis Kepatuhan terhadap GMP
Pengurangan Mikroba Reduksi 6-Log (spora Bacillus atrophaeus) Sesuai persyaratan ISO 14644-4 dan EU GMP Annex 1.
Konstruksi Ruang (Chamber) SUS304/316L dengan permukaan yang dipoles elektro (electropolish) (Ra < 0,4 µm) Kompatibilitas penuh dengan lingkungan ISO Kelas 1 hingga Kelas 7.
Teknologi Kontrol Otomasi servo Fanuc dengan redundansi PLC ganda & layar sentuh HMI Operasi tervalidasi sesuai peraturan FDA 21 CFR Part 11.

Integrasi Komprehensif

Menawarkan keahlian mendalam dalam sistem cleanroom, Farclean menyediakan dokumentasi validasi teknik lengkap, mulai dari Kualifikasi Desain (DQ), Kualifikasi Instalasi (IQ), Kualifikasi Operasional (OQ), hingga Kualifikasi Kinerja (PQ), memastikan persetujuan peraturan yang cepat dan integrasi yang lancar dengan infrastruktur cleanroom Anda yang ada.

Berkonsultasilah langsung dengan teknisi pintu cleanroom kami untuk interlock tata letak yang optimal dan sinkronisasi kaskade tekanan yang disesuaikan.

Pertanyaan yang Sering Diajukan (FAQ)

Apa keunggulan utama Dynamic Pass Box dibanding Static Pass Box?

Dynamic Pass Box dilengkapi dengan sistem tata udara mandiri berupa Fan Filter Unit (FFU) berfilter HEPA H14 dan sirkulasi udara laminar vertikal (0,36–0,54 m/s). Udara bersih ini aktif menyapu dan membersihkan debu mikroskopis serta partikel dari permukaan material selama proses transfer antar zona dengan tingkat kebersihan berbeda (misalnya dari Grade C ke Grade B/A).

Bagaimana sistem interlock pintu mencegah kontaminasi silang?

Pass box dilengkapi sistem interlock elektronik berbasis mikroprosesor. Ketika satu pintu dibuka, pintu di sisi seberang secara otomatis terkunci rapat. Setelah pintu ditutup, sistem dapat mengaktifkan siklus pembersihan udara (purging) dan sterilisasi UV selama durasi waktu terprogram sebelum pintu kedua diizinkan untuk dibuka.

Apakah unit ini dilengkapi sertifikasi validasi farmasi (DQ/IQ/OQ/PQ)?

Ya, setiap unit dynamic pass box Farclean disuplai dengan dokumen validasi komprehensif (DQ, IQ, OQ, PQ), sertifikat uji kebocoran filter HEPA (test report), dan sertifikasi material baja tahan karat SUS304 / SUS316L untuk keperluan audit cGMP dan EU GMP.

Tabel Spesifikasi Teknis Lengkap

Material Ruang (Chamber) Baja Tahan Karat SUS304 / SUS316L dengan Interior Electropolish (Ra < 0,4 µm)
Efisiensi Filtrasi Udara Segel Gel HEPA H14 (99,995% @ 0,3 µm) dengan Port Uji G4 + Pra-filter
Kecepatan & Pola Aliran Udara 0,36–0,54 m/s Aliran Laminar Vertikal Seragam (ISO Kelas 5 / Grade A at rest)
Kemampuan Reduksi Mikroba Reduksi 6-Log (spora Bacillus atrophaeus) tervalidasi untuk GMP Annex 1
Aktuasi & Interlock Pintu Pintu geser elektrik otomatis / Interlock elektromagnetik fail-safe (gagal-aman)
Arsitektur Kontrol Siemens / Fanuc PLC dengan panel sentuh HMI berwarna yang sesuai dengan FDA 21 CFR Part 11
Sterilisasi Pembasmi Kuman UV Lampu UV-C 253,7 nm dengan pengatur waktu interlock dan mekanisme pemadaman otomatis yang aman
Pemantauan Diferensial Tekanan Pengukur tekanan diferensial magnetik (0–250 Pa / 0–500 Pa)
Peringkat Daya & Akustik 220V / 50Hz / 1 Fase | Motor blower EC berkebisingan rendah < 62 dB(A)

Butuh Spesifikasi Khusus atau Proyek Terpadu?

Konsultasikan kebutuhan pass box dinamis kustom, sistem interlock, sterilisasi UV/VHP, atau fasilitas cleanroom cGMP Anda dengan tim ahli kami di Indonesia.

Custom Dynamic Pass-Through Box Manufacturer for GMP Grade A Cleanrooms – PT Far Clean Indonesia
GMP Grade A Dynamic
6-Log Kill Reduction & GMP Annex 1 Validation

Designed specifically for pharmaceutical and biotechnology sterile facilities with proven 6-log microbial reduction and FDA 21 CFR Part 11 compliance.

Sterile Cleanroom Equipment ID: fc-passbox-dynamic
Custom Dynamic Pass-Through Box Manufacturer for GMP Grade A Cleanrooms

Advanced Aseptic Material Transfer Chambers with HEPA H14 & 6-Log Microbial Reduction

Farclean is a trusted custom dynamic pass-through box manufacturer, delivering advanced encapsulation solutions for GMP Grade A pharmaceutical, biologics, and life sciences cleanrooms.

Industrial Application Recommendations:

GMP Grade A Aseptic Filling Suites Biologics & Vaccine Manufacturing Active Pharmaceutical Ingredients (API) BSL-3/BSL-4 Containment Laboratories Medical Device Sterile Packaging

Key Advantages & Features:

  • ✓ Electrically Actuated Sliding Mechanism: Piston servo-based automatic door system for hands-free operation.
  • ✓ 6-Log Microbial Reduction: Proven to eradicate Bacillus atrophaeus spores according to ISO 14644-4 and EU GMP Annex 1 standards.
  • ✓ Variable Cycle Sequencing: PLC controlled Dehumidification, Sterilization, Transfer and Exhaust automation cycles.
  • ✓ Advanced Catalytic Filtration: Built-in catalytic filtration system breaks down sterilization agent residues for operator safety.

* Customization of chamber dimensions, electropolished SUS304 / SUS316L material options, port integration, and BMS / SCADA connectivity.

cGMP Grade A Aseptic Transfer Solution

Custom Dynamic Pass-Through Box Manufacturer for GMP Grade A Cleanrooms

GMP Grade A cleanroom environments demand precise surface sterilization measures before biological products, active pharmaceutical ingredients, or other sensitive goods enter manufacturing lines. As a specialized custom dynamic pass-through box manufacturer, Farclean designs and builds automated transfer enclosures engineered for complete microbial reduction and seamless integration with your cleanroom infrastructure including validated cleanroom doors and precision modular wall panels.

Custom Dynamic Pass-Through Box Manufacturer for GMP Grade A Cleanrooms – PT Far Clean Indonesia

Innovative Transfer Chamber Design and Operation

Farclean dynamic pass-through boxes feature cutting-edge sterilization technology and versatile packaging solutions tailored to the most rigorous contamination control standards, ensuring your products maintain integrity throughout transfer:

01

Electrically Actuated Sliding Mechanism

Our patented piston-driven door system enables full hands-free operation, eliminating human intervention and potential cross-contamination for highly biosafety-sensitive facilities.

02

Modular Wall Panel Integration

Available as freestanding units or designed to interface seamlessly with cleanroom wall systems, allowing optimal configuration for product handling protocols.

03

Variable Cycle Sequencing

Customizable automation cycles precisely manage Dehumidification, Sterilization, Transfer, and Exhaust phases for zero or low bio-burden transfer between distinct cleanroom environments.

04

Advanced Catalytic Filtration

Integrated filter systems break down residual sterilizing agents, ensuring complete safety and environmental compliance in GMP settings.

05

Basketry Enclosure Options

Available with interchangeable, sterilized material holders designed for long-life integration with our durable cleanroom wall panels.

Dynamic Pass-Through Box Performance Metrics

System Parameters Technical Specifications GMP Compliance
Microbial Reduction 6-log kill reduction (Bacillus atrophaes spores) Conforms to ISO 14644-4 and EU GMP Annex 1 requirements.
Chamber Construction Type 304/316L SS with electropolished surfaces (Ra < 0.4 µm) Full compatibility with ISO Class 1 to Class 7 environments.
Control Technology Fanuc servo automation with dual redundant PLC & HMI touch display Validated operations meeting FDA 21 CFR Part 11 regulations.

Comprehensive Turnkey Integration

Boasting deep expertise in cleanroom systems, Farclean provides full engineering validation documentation, from Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), to Performance Qualification (PQ), ensuring rapid regulatory approval and seamless integration with your existing cleanroom infrastructure.

Interface directly with our specialized cleanroom doors engineers for optimum layout interlocking and customized pressure cascade synchronization.

Frequently Asked Questions (FAQ)

What are the main advantages of Dynamic Pass Box over Static Pass Box?

The Dynamic Pass Box is equipped with an independent air system in the form of a Fan Filter Unit (FFU) with HEPA H14 filter and vertical laminar air circulation (0.36 - 0.54 m/s). This clean air actively sweeps and cleans microscopic dust and particulates from the material surface during the transfer process between zones with different cleanliness levels (for example from Grade C to Grade B/A).

How does a door interlock system prevent cross contamination?

The pass box is equipped with a microprocessor electronic interlock system. When one door is opened, the door on the opposite side automatically locks tightly. Once the door is closed, the system can activate air purging and UV sterilization cycles for a programmed duration of time before the second door is allowed to be opened.

Does this unit have pharmaceutical validation certification (DQ/IQ/OQ/PQ)?

Yes, each Farclean dynamic pass box unit is supplied with comprehensive validation documents (DQ, IQ, OQ, PQ), HEPA filter leak test certificate ( test report), and SUS304 / SUS316L stainless steel material certification for FDA/GMP and EU GMP cGMP audit purposes.

Complete Technical Specifications Table

Chamber Materials SUS304 / SUS316L Stainless Steel with Electropolished Interior (Ra < 0.4 µm)
Air Filtration Efficiency Gel-seal HEPA H14 (99.995% @ 0.3 µm) with Pre-filter G4 + Test Ports
Airflow Velocity & Pattern 0.36 – 0.54 m/s Uniform Vertical Laminar Flow (ISO Class 5 / Grade A at Rest)
Microbial Reduction Capability 6-Log kill reduction (Bacillus atrophaeus spores) validated for GMP Annex 1
Door Actuation & Interlock Electrically actuated automated sliding doors / Electromagnetic fail-safe interlock
Control Architecture Siemens / Fanuc PLC with color HMI touch panel compliant with FDA 21 CFR Part 11
UV Germicidal Sterilization 253.7 nm UV-C lamp with interlock timer and safety auto-shutoff mechanism
Pressure Differential Monitoring Magnehelic differential pressure gauge (0–250 Pa / 0–500 Pa)
Power & Acoustic Ratings 220V / 50Hz / 1 Phase | Low-noise EC blower motor < 62 dB(A)

Need Custom Specifications or Turnkey Project?

Consult your needs for custom dynamic pass boxes, interlock systems, UV/VHP sterilization, or cGMP cleanroom facilities with our expert team in Indonesia.

Konsultasi Cepat WhatsApp