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.
A real manufacturer, with our own plant in Shanghai
In-house design, fabrication and assembly — from stainless-steel barrier systems to VHP sterilization equipment.



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.

Aseptic filling, sterility testing, high-containment (OEB5) and cell-processing isolators, plus open RABS. 6 models.
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Portable and HVAC-integrated VHP systems for validated 6-log bio-decontamination of rooms, airlocks and equipment. 5 models.
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VHP and biosafety pass boxes, airtight doors, containment dampers and sterile transfer valves. 10 models.
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BIBO filter housings, safe-change exhaust units, and laminar airflow hoods, trolleys and booths. 7 models.
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Mist shower rooms and BSL-3 decontamination showers for safe garment and personnel entry/exit. 2 models.
See all →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.
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.
Industries We Serve
Contamination-control and containment equipment for the most demanding pharmaceutical and life-science processes.
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.















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