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Superior Quality ABS Lateral Flow Rapid Plastic Test Kit Empty Cassette
US$0.05-0.20
10,000 Pieces
Sample price:US$0.50/piece.Request sample

Product profile

Customization

Available

Type

IVD Reagent

Shelf Life

Two Years

Model NO.

DLM-5.5

Format

Cassette/Midstream

Color

White/Red/Blue/Customized

Transport Package

Plastic Bag, Sealed Carton

Specification

5.5mm

Trademark

OEM/ Neutral

Origin

China

HS Code

3923300000

Production Capacity

300000 PCS/Month

Company profile

Business Type: Manufacturer/Factory, Trading Company CertifiedNearest Port: Shanghai Port, Beijing PortAverage Response Time: ≤3.52h CertifiedTerms of Payment: LC, T/T, D/P, etc. CertifiedInternational Commercial Terms(Incoterms): FOB, CIF, CFR

AI-Powered supplier vetting

SummaryHebei Times Medical Technology Co., Ltd. is identified as a China-based manufacturer/factory engaged in medical devices and in vitro diagnostic reagents, including urine test strips, infectious disease tests, uncut sheets, and related raw materials. The supplier reports ISO 9001 certification, 21–30 years of combined R&D engineer experience, 50 quality-control staff, and five production lines. It states that it has 14 years of industry experience, a mature supply chain, and partners in more than 50 countries, with customer deployments across multiple regions. However, the available trade records show only one transaction per listed period and a single associated buyer in Vietnam, so the breadth of independently evidenced customer cases and trading history remains limited. Evidence is insufficient to assess financial credibility, customization capability, or after-sales service in detail.
Supplier typeThe supplier is explicitly identified as Hebei Times Medical Technology Co., Ltd., a manufacturer/factory based in Hebei, China. Its stated business focuses on the research, development, and sales of medical devices and in vitro diagnostic reagents.
CertificationsThe supplier reports holding ISO 9001 certification. This provides explicit evidence of a certified quality-management system, although no additional certifications are stated.
R&D capabilityThe company states that it conducts research and development in medical devices and in vitro diagnostic reagents, and reports 21–30 years of total R&D engineer experience. Its product scope includes diagnostic tests and home-diagnosis products, supporting an R&D presence, but no specific patents, new-product results, or documented innovation achievements are provided.
Production capacityThe supplier is classified as a manufacturer/factory and reports five production lines, 50 quality-control staff, a mature supply chain, and quality control covering semi-finished products, plastic parts, accessories, and production equipment. These stated resources support production capability, although actual capacity utilization and delivery performance are not documented.

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