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VHP Sterilization

HVAC-Integrated VHP System

Vaporized hydrogen peroxide bio-decontamination built directly into your HVAC system — a reproducible 6-log reduction across rooms, airlocks and equipment, dry and residue-free once aeration is complete.

6-Log ReductionResidue-FreeSiemens PLC Control
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Fenggu HVAC-Integrated VHP System FGVHP1000
Isolators

Aseptic Filling Isolator

A fully enclosed Grade A (ISO 5) barrier for sterile filling, stoppering and capping. Integrated VHP bio-decontamination delivers a validated, residue-free 6-log reduction before every campaign.

Grade A / ISO 56-Log VHP DecontaminationH14 HEPA Filtration
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Fenggu Aseptic Filling Isolator
Isolators

Negative Pressure Isolator

A sealed negative-pressure barrier that protects the operator and environment when handling potent, cytotoxic, sensitizing or infectious materials — inward airflow with single-pass HEPA exhaust for OEB4/OEB5 containment.

OEB4 / OEB5 ContainmentNegative PressureHEPA Single-Pass Exhaust
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Fenggu Negative Pressure Isolator
Isolators

Sterility Test Isolator

A stable Grade A (ISO 5) environment for pharmacopoeia sterility testing — protecting the sample from false positives and the operator from the tested product, with integrated VHP 6-log decontamination.

USP 1208 ValidatedGrade A / ISO 5Dual-Chamber Design
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Fenggu Sterility Test Isolator
Isolators

Open RABS (oRABS)

A restricted-access barrier system providing a Grade A zone with positive-pressure laminar flow over aseptic filling and processing lines.

Grade A / ISO 5Positive-Pressure Laminar FlowRestricted Access
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Fenggu Open RABS Isolator
Transfer & Containment

VHP Pass Box

Wall-mounted transfer chamber with integrated VHP for residue-free 6-log surface decontamination between classified areas.

6-Log DecontaminationResidue-FreeWall-Mounted
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Fenggu VHP Pass Box
5PRODUCT CATEGORIES
30+EQUIPMENT MODELS
6-LogVHP BIO-DECONTAMINATION
H14HEPA FILTRATION
SUS316LPRODUCT-CONTACT SURFACES
About Fenggu

Barrier & Sterilization Equipment, Engineered to cGMP

Shanghai Fenggu Medical Equipment Co., Ltd. designs and manufactures pharmaceutical isolators, VHP sterilization systems, pass boxes, airtight doors and cleanroom containment equipment for sterile and high-containment processing. From a single unit to a complete turnkey suite, we engineer each system to your process — containment level, throughput and validation requirements — and support it from design and manufacturing through factory acceptance testing, installation and validation.

cGMP Compliant

Designed and documented to cGMP and FDA expectations.

One-Stop Solution

From single equipment to complete turnkey sterilization systems.

Customization

Tailored dimensions, materials and configurations to your process.

Export Ready

Experienced in international delivery, documentation and validation support.

Our Facility

A real manufacturer, with our own plant in Shanghai

In-house design, fabrication and assembly — from stainless-steel barrier systems to VHP sterilization equipment.

Shanghai Fenggu Medical Equipment facility
Our Shanghai facility
Fenggu VHP equipment production workshop
Production workshop
Fenggu engineering and administrative office
Engineering & office

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Cleanroom & Containment Equipment

Five product categories, 30+ models — from aseptic and high-containment isolators to VHP sterilization, transfer and containment devices, air handling and personnel decontamination.

Fenggu isolators and barrier systems
Isolation & Barrier Systems

Aseptic filling, sterility testing, high-containment (OEB5) and cell-processing isolators, plus open RABS. 6 models.

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Fenggu HVAC-integrated VHP sterilization system
VHP Sterilization

Portable and HVAC-integrated VHP systems for validated 6-log bio-decontamination of rooms, airlocks and equipment. 5 models.

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Fenggu VHP pass box for sterile transfer
Transfer & Containment

VHP and biosafety pass boxes, airtight doors, containment dampers and sterile transfer valves. 10 models.

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Fenggu BIBO filter housing
Air Handling & Filtration

BIBO filter housings, safe-change exhaust units, and laminar airflow hoods, trolleys and booths. 7 models.

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Fenggu mist shower room for personnel decontamination
Personnel Decontamination

Mist shower rooms and BSL-3 decontamination showers for safe garment and personnel entry/exit. 2 models.

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Technology

How VHP Bio-Decontamination Works

Vaporized hydrogen peroxide (VHP) is the standard for validated bio-decontamination in modern pharmaceutical manufacturing. A VHP cycle distributes hydrogen peroxide vapor evenly across every surface of an enclosed space — isolators, pass boxes, RABS and cleanrooms — achieving a reproducible 6-log reduction of microbial contamination, with no chemical residue once aeration is complete.

At Fenggu, VHP generation is integrated directly into our isolators and pass boxes rather than added as an afterthought — giving operators precise control over cycle time, concentration and distribution.

1
Dehumidification
2
Conditioning
3
Decontamination
4
Aeration
Fenggu HVAC-Integrated VHP System
Technology

Biosafety Airtight Sealing

In BSL-3/4 laboratories and containment suites, airtightness is the last line of defense. Fenggu gastight doors, biosafety pass boxes and containment valves are built and pressure-tested to hold — with high-density EPDM seals resistant to VHP, formaldehyde and chlorine dioxide. These are measured, verifiable numbers, not marketing claims.

0.024%Minute leak rate — mechanical-compression airtight door
5,000+Open/close cycles, still bubble-tight — biosafety valve
±2000 PaLeak ≤ 0.1%/min — BIBO filter housing
≥2500 PaStructural pressure resistance — gastight doors

Industries We Serve

Contamination-control and containment equipment for the most demanding pharmaceutical and life-science processes.

Sterile Injectables
Biologics & Vaccines
Cell & Gene Therapy
API & HPAPI Handling
BSL-3 / BSL-4 Laboratories
Sterile Compounding
Our Clients

Trusted by leading pharmaceutical & life-science organizations

Fenggu isolation, VHP sterilization and containment equipment serves major pharmaceutical groups, cell & gene therapy companies, hospitals and research institutes across China.

CSPC Pharmaceutical Group
BeiGene
Sinopharm
Pigeon
PELL BMT
The First Hospital of China Medical University
Wuhan Healthgen (Oryzogen)
Sichuan Zitonggong Pharmaceutical
Chinese Academy of Sciences
Cangzhou Xubidi Pharmaceutical
Shandong Institute for Food and Drug Control
Qilu Pharmaceutical
Harbin Peiqilong Bio
Beijing Institute of Technology
IMEIK Technology
& many more
Featured Case Study

HVAC-Integrated VHP at a CSPC mRNA Vaccine Facility

See how Fenggu engineered a VHP sterilization system directly into the HVAC of CSPC Megalith Biopharmaceutical’s Qinhuangdao mRNA vaccine facility — replacing multiple mobile VHP units with one centralized, automated system serving three sterile areas.

Read the Case Study →

FGVHP1000 HVAC-integrated VHP sterilization system at CSPC Megalith Biopharmaceutical Qinhuangdao facility

Certifications & Credit Ratings

Independently assessed and rated AAA for quality, service and enterprise credit.

AAA Quality Oriented and Trustworthy Enterprise AAA Quality Service Integrity Unit AAA Honest Supplier Enterprise AAA Enterprise Credit Rating Certificate AAA Enterprise Abiding by Contracts and Keeping Promises AAA Service Oriented and Trustworthy Enterprise

Engineered to International Standards

Our equipment is designed and documented to the standards global pharmaceutical manufacturers rely on.

cGMP
FDA 21 CFR Part 11
EU GMP Annex 1
ISO 14644
HEPA H14
ISO 10648-2

Frequently Asked Questions

How do I select the right isolator for my application?

Isolator selection depends on your process risk and containment goal. Aseptic isolators protect the product in sterile filling and compounding; cRABS suit aseptic filling lines that need frequent operator interaction; OEB (high-containment) isolators protect operators when handling potent or toxic compounds. Share your process, OEB level and throughput, and our engineers will recommend a configuration.

Are your systems cGMP and FDA compliant?

Yes. Our isolators, VHP systems and pass boxes are designed and documented to cGMP requirements and FDA expectations, including material traceability, HEPA H14 filtration and full validation documentation (IQ/OQ support available).

Do you provide installation and validation support?

Yes. We support the full lifecycle — design, manufacturing, factory acceptance testing (FAT), on-site installation, and validation documentation to help your team complete IQ/OQ/PQ.

Do you export and support overseas projects?

Yes. We have experience with international delivery, export documentation and remote/on-site commissioning support for pharmaceutical clients in overseas markets.

Ready to Start Your Project?

Tell us your process, containment level and throughput — our engineers will recommend a configuration and quote.

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