What is the lead time for production?

Peak season lead time is 1-3 months, while off-season is one month.

What certifications does the manufacturer hold?

The company operates under the ISO13485 Quality Management system.

Double Person Vertical Air Flow Clean Bench

Name: Double Person Vertical Air Flow Clean Bench
Brand: Ningbo Cbmtec Medical Equipment Co., Ltd.
SKU: 2171289755

Zhejiang, ChinaNingbo Cbmtec Medical Equipment Co., Ltd.

US$450.00-530.00

1 Piece

Product profile

Customization

Available

Clean Grade

Grade 100(209e U.S. Federal)

Air Supply

Vertical

Inside Size

880*650*580mm

Outside Size

1040*690*1600mm

Power

AC 220V/50Hz

Equiblast Speed

0.25-0.45m/S

Usage

Research Institute, Lab

Clean Level

Class 100

Transport Package

Wooden

Specification

Vertical Flow Clean Bench

Trademark

CBMTEC

Origin

Zhejiang, China

HS Code

8414609090

Production Capacity

1000PCS/Month

Key features

Grade 100 Cleanliness: Meets Class 100 (209e U.S. Federal) standards for critical environments.

Vertical Air Flow: Unidirectional airflow design ensures optimal contamination control.

Adjustable Wind Speed: Contact switch adjusts voltage to maintain ideal wind speed (0.25-0.45m/s).

Movable Door System: Spring up/down doors allow flexible positioning and air insulation.

304 Stainless Steel: Durable work area material resistant to corrosion and easy to clean.

LED Panel Control: User-friendly operation interface for monitoring and control.

ISO13485 Certified: Manufactured under strict quality management system for medical use.

Custom Specifications: Non-standard clean bench specifications available upon demand.

Company profile

Ningbo Cbmtec Medical Equipment Co., Ltd.

Zhejiang, China

Business Type: Manufacturer/FactoryExport Year: 2015-10-08Nearest Port: NingboAverage Response Time: ≤3.95hTerms of Payment: LC, T/T, D/P, etc.International Commercial Terms(Incoterms): FOB, EXW, CFR, CIF, DAT, FAS, DDP, DAP, CIP, CPT, Others, FCA

AI-Powered supplier vetting

SummaryNingbo Cbmtec Medical Equipment Co., Ltd. is identified as a China-based manufacturer/factory operating in Zhejiang and supplying medical and industrial equipment. It reports 10 production lines, 11–20 years of total R&D-engineer experience, and 6–10 quality-control staff. Its product scope includes patient monitors, ventilators, patient lifts, anesthesia machines, ultrasound scanners, gas cylinders, oxygen concentrators, pulse oximeters, and oxygen regulators. The supplier reports BSCI, ISO 9001, and ISO 14001 management-system certifications, and began exporting in 2015, with 51%–70% of sales from exports. Evidence is insufficient to confirm after-sales service, customer cases, customization capability, or financial credibility. The available information supports manufacturing capacity and an established R&D and quality-control structure, but does not independently verify the stated quality guarantee or certification scope.

Supplier typeThe supplier is explicitly identified as a Manufacturer/Factory, with a limited-company structure and a stated factory address in Ningbo, Zhejiang, China. This directly supports classification as a manufacturing supplier rather than only a trading intermediary.

CertificationsThe supplier reports BSCI, ISO 9001, and ISO 14001 certifications under supplier management systems. These certifications are stated in the provided information, although the slices do not provide certificate numbers, validity dates, or scopes.

R&D capabilityThe supplier reports 11–20 years of total R&D-engineer experience and states that it has its own R&D and technical engineers. This supports an established internal technical base, but the slices do not document patents, proprietary technologies, new-product launches, or measurable innovation outcomes.

Production capacityThe supplier reports 10 production lines, 6–10 quality-control staff, and its own manufacturing facilities, while offering a broad range of medical and industrial equipment. These facts support operational manufacturing capability; however, the stated annual output is limited to the category reported and no capacity-utilization or delivery-performance evidence is provided.