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Class 2 Biosafety Cabinet: Reliable Choice for Lab Safety Operations
US$1,200.00
1-9 Pieces
US$800.00
10+ Pieces
Product profile
Customization
AvailableCertification
CE, ISO9001Usage
Research Institute, Hospital, School, Company, Clean RoomNoise
≤62DBType
Vertical Flow Clean BenchPower
220V/50HzAir Velocity
0.35-0.55m/SMaterial
Working Area: 304 Stainless SteelColor
WhiteFront Window
Motorized. Toughened Glass . Anti UV.Function
Purification FilterDown Flow Velocity
0.35 M/S(68.88FPM/64.94FPM)Filtration Grade
H13/H14Main Body
Cold-ROOpening Height
200 mm-370mm 200 mm-370 mmLED Lamp
8W*2Transport Package
Export Wooden CaseSpecification
1200/1500/1800/2000*795*2050 mmTrademark
SUZHOU PHARMA MACHINERYOrigin
ChinaHS Code
842139909Production Capacity
50sets/WeekKey features
Class II Biosafety Protection: Provides personnel, product, and environmental protection with HEPA filtration.
H13/H14 Filtration Grade: Advanced HEPA filters ensure high-efficiency removal of hazardous particles.
Motorized Front Window: Toughened anti-UV glass with motorized control for ergonomic operation.
Stainless Steel Construction: Working area made of 304 stainless steel for durability and easy cleaning.
CE and ISO9001 Certified: Complies with international safety and quality management standards.
OEM and ODM Services: Offers full customization, flexible customization, and sample-based customization.
Versatile Laboratory Use: Ideal for microbiology, pharmaceuticals, cell culture, and educational research.
Company profile
CertifiedBusiness Type: Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Customization from Samples, Full Customization, etc. CertifiedExport Year: 9 Years CertifiedNearest Port: Shanghai PortAverage Response Time: ≤1.31h
AI-Powered supplier vetting
SummaryThe supplier is identified as a manufacturing factory in Suzhou, China, supplying pharmaceutical machinery, packaging machinery, cleanroom equipment and materials, laboratory equipment, and related products. It provides 3D software design, ODM, OEM, SDK, and multiple customization options, indicating broad technical and customization capabilities. Production evidence includes a stated annual cleanroom capacity of 10,000 square meters and a 500 m² manufacturing plant, with most materials reportedly stocked and shipment possible within seven days except for specially made air conditioners. Quality assurance is stated, but documented service procedures, complaint-handling records, corrective actions, and approved-supplier lists are absent. No overseas warehouse, showroom, agents, branches, or offline trade-show participation are reported. No new products were developed in the past year. Customer project experience is described for national and international pharmaceutical and laboratory projects, but...
Supplier typeThe supplier is explicitly classified as a factory and operates in manufacturing and processing, with business scope covering pharmaceutical machinery, packaging machinery, cleanroom equipment, water treatment equipment, laboratory equipment, and related products. This supports classification as a specialized industrial equipment manufacturer rather than only a trading company.
After-Sales capabilityThe supplier has quality assurance, but reports no written procedures or records for service assessment, corrective and preventive actions, or effective customer-complaint handling. It also has no overseas warehouse, showroom, agents, or branches, limiting demonstrated overseas service infrastructure.
R&D capabilityThe supplier is identified as a professional technical supplier, provides 3D software design, ODM services, OEM services for well-known brands, and an available SDK. However, it also reports no new products during the past year, so current innovation output is mixed rather than consistently demonstrated.
Production capacityThe supplier states annual cleanroom productivity of 10,000 square meters, operates a 500 m² manufacturing plant, and reports fast production with most materials stocked and shipment within seven days except for specially made air conditioners. These statements provide explicit evidence of production capacity and responsiveness, although the capacity data covers cleanrooms rather than every product category.
Customization capabilityThe supplier offers customization from samples, full customization, and flexible customization, together with 3D software design, ODM, OEM, and customized tools and parts. Its broad cleanroom and pharmaceutical equipment scope further supports the ability to deliver tailored industrial solutions.
Product Q&A
Q:What is the difference between Class I, II, and III biosafety cabinets?
A:
Class I protects only the product. Class II protects personnel, product, and environment. Class III (glove boxes) offers maximum containment for highly infectious agents.
Q:What is the air velocity inside the cabinet?
A:
The down flow velocity is 0.35-0.55 m/s, and the front suction wind speed is 0.55 m/s.
Q:Does the cabinet support customization?
A:
Yes, we offer full customization, flexible customization, and customization from samples via OEM and ODM services.
Q:What is the lead time for orders?
A:
The average lead time is one month for both peak and off-peak seasons.
Q:What certifications does the product have?
A:
The product is certified with CE and ISO9001 standards.
Send Inquiry
*To:
Suzhou Pharma Machinery Co., Ltd.
Suzhou Pharma Machinery Co., Ltd.*Content:
Supplier replies will be sent to your registered email
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