Bm® Disposable High Quality Medical Endoscope Sputum Specimen Trap

Name: Bm® Disposable High Quality Medical Endoscope Sputum Specimen Trap
Brand: ZHEJIANG BAITE MEDICAL APPLIANCES CO., LTD.
SKU: 2142021435

Zhejiang, ChinaZHEJIANG BAITE MEDICAL APPLIANCES CO., LTD.

US$0.05-0.08

1,000 Pieces

Sample price:US$0.00/piece.Request sample

Product profile

Customization

Available

Type

Drainage Container/Tube, Face Mask/Apron/Gloves

Material

Plastic

Ethylene Oxide Sterilization

Quality Guarantee Period

Two Years, Three Years

Group

All

Logo Printing

Without Logo Printing

Transport Package

Cartons

Specification

customized

Trademark

Origin

China

HS Code

90183900

Production Capacity

100000000000

Company profile

High Repeat Buyers ChoiceYears of Export ExperienceProduct CertificationEnvironmental Protection

ZHEJIANG BAITE MEDICAL APPLIANCES CO., LTD.

Zhejiang, China

Business Type: Manufacturer/Factory, Group CorporationExport Year: 1998-08-08Nearest Port: Shanghai, NingboAverage Response Time: ≤4.38hTerms of Payment: LC, T/T, D/P, etc.International Commercial Terms(Incoterms): FOB, CFR, CIF

AI-Powered supplier vetting

SummaryThe supplier operates in medical-device production and sales, including Class I, Class II, and potentially Class III devices subject to approval. It offers OEM, ODM, and broad customization services, has reported new-product activity within the past year, and exports 90% of total sales with 26 years of export experience. Production-related evidence includes an automatic assembly line, sterilization equipment, in-stock capability, and seven quality assurance/control inspectors. Service procedures for corrective and preventive actions and customer complaints are documented and followed. However, the supplier reports no quality assurance in quality control processes, no valid manufacturing contract with affiliated subcontractors, no overseas warehouse, no overseas agents or branches, and no available SDK. Financial credibility, formal certifications, and identifiable customer cases are not sufficiently evidenced.

Supplier typeThe supplier is identified as a combined company and operates in medical-device manufacturing and sales. Its stated scope includes Class I and Class II devices, while Class III production and operation require approval; the business scope also includes import and export activities subject to applicable approvals.

After-Sales capabilityThe supplier has documented and followed procedures for corrective and preventive actions and customer complaints, supporting a defined service process. However, it has no overseas agents or branches, no overseas warehouse, and reports service coverage in zero countries, limiting evidence of international after-sales reach.

R&D capabilityThe supplier reports new products within the past year and provides ODM services, indicating active product-development capability. It also reports no available SDK, so technical-development support involving an SDK is not demonstrated.

Production capacityProduction capability is supported by medical-device manufacturing scope, an automatic assembly line, sterilization equipment, in-stock capability, seven quality assurance/control inspectors, and standardized finished-product inspection instructions. Offsetting concerns include the stated absence of quality assurance in quality-control processes and no valid contract with affiliated subcontractors.

Customization capabilityThe supplier explicitly offers customization from samples, full customization, customization from designs, minor customization, and flexible customization. These capabilities are stated consistently in both R&D and design-service records.