What is the power consumption?

Power consumption ranges from 700W to 950W depending on the model.

Laboratory Super Clean Bench Vertical Laminar Flow Cabinet with Ce

Name: Laboratory Super Clean Bench Vertical Laminar Flow Cabinet with Ce
Brand: Zhengzhou Hepo International Trading Co., Ltd.
SKU: 694666402

Henan, ChinaZhengzhou Hepo International Trading Co., Ltd.

Negotiable

1 Piece

Product profile

Customization

Available

Certification

Usage

Research Institute, Hospital, School, Company

Model NO.

DXC-V3

Noise

≤60dB

Type

Vertical Flow Clean Bench

Usage Person

External Size (WDH)

1000*730*1680mm

Operation Size (WDH)

920*675*640

Air Velocity

0.3m/S ~ 0.6m/S,Adjustable by Six Channels

Clean Rate

100 Class for USA209e

Illuminating Value

≥1000lux

Power

700W

Net Weight

105kgs

Name

Vertical Laboratry Laminar Flow Cabinet

Transport Package

Standard Exporting Packing

Specification

ISO9001, SGS

Trademark

HEPOBIO

Origin

China

Production Capacity

10000sets/Year

Key features

CE Certified Safety: Complies with CE standards for safe laboratory operations.

100 Class Cleanliness: Achieves 100 Class clean rate according to USA209e standard.

Adjustable Air Velocity: Air velocity adjustable from 0.3m/s to 0.6m/s via six channels.

High Efficiency Filtration: Uses H13 or H14 HEPA filters with polyester pre-filters.

Durable Steel Construction: Cold-rolled steel body with anti-bacteria coating and stainless steel table.

Advanced Control System: Pure English digital display with bactericidal timing and memory functions.

Long Life UV Lamp: Equipped with new non-ozone UV lamps for high strength and longevity.

Company profile

Zhengzhou Hepo International Trading Co., Ltd.

Henan, China

Business Type: Manufacturer/Factory, Trading Company, Group CorporationAverage Response Time: ≤3.20h

AI-Powered supplier vetting

SummaryThe supplier presents established manufacturing and quality-system credentials, with eight production lines, stated output across five medical-equipment categories, broad export coverage, and ISO 13485, ISO 9001, ISO 14001, and GMP certifications. It offers extensive product customization and maintains inventory capability, with stated lead times within 15 working days in both peak and off-season periods. However, evidence also shows material gaps: no written corrective-action or complaint-handling procedures, no documented service-assessment procedure, no environmental impact assessment report, no overseas warehouse or showroom, no recent new-product activity, no ODM or major-brand OEM service, no SDK, zero stated R&D patents, and no available R&D design-control documentation. Financial records are indicated for multiple years, but the slices do not provide sufficient non-financial evidence to assess financial credibility.

Supplier typeThe supplier manufactures medical and biosafety-related equipment, including cold-chain, clinical, first-aid, and laboratory products. It operates eight production lines, describes imported production equipment, and exports to multiple global regions, indicating a manufacturer with broad product and market coverage.

CertificationsThe supplier states that its factories adopted ISO 9001:2008 and ISO 13485 systems, while its supplier-management certifications include ISO 13485, ISO 9001, ISO 14001, and GMP. These explicitly stated certifications support a positive assessment of formal quality and management-system coverage.

R&D capabilityThe supplier has 11–20 years of total R&D-engineer experience and can customize products, but reports no new products during the past year, no SDK, no software-instrument R&D, zero R&D patents, and no available design-input, output, review, verification, or validation documentation. The explicit evidence indicates limited demonstrated innovation infrastructure.

Production capacityThe supplier operates eight production lines and reports production quantities for deep freezers, analyzers, and incubators, alongside inventory capability and broad export markets. Its company description also cites dedicated product solutions and imported production equipment, providing explicit evidence of substantial manufacturing capability.

Customization capabilityThe supplier explicitly offers customization from samples and designs, full, minor, and flexible customization, and assigns R&D engineers to customize products according to customer needs. However, the absence of documented R&D design-control records means process formalization is not demonstrated, while the customization offering itself is clearly supported.