What quality certifications does the company hold?

We have passed ISO9001:2015 and ISO13485 certifications.

Is OEM service available?

Yes, OEM service is available for our customers.

What is the inspection process for finished products?

We perform 100% inspection including visual and functional checks on all finished products.

Xinke Desorb II Sdg II Suitable for Stgo Sta Series Coagulation Analyzer

Name: Xinke Desorb II Sdg II Suitable for Stgo Sta Series Coagulation Analyzer
Brand: Zhejiang Xinke Medical Technology Co., Ltd.
SKU: 2159264925

Zhejiang, ChinaZhejiang Xinke Medical Technology Co., Ltd.

US$1.00

1 Piece

Sample price:US$1.00/piece.Request sample

Product profile

Customization

Available

Type

IVD Reagent

Transport Package

Carton

Model NO.

JXK-420

Specification

15ml

Trademark

xinke

Origin

China

HS Code

3822190090

Production Capacity

500000/Ctns

Key features

100% Analyzer Compatibility: Reagents are fully compatible with STGO STA Series Coagulation Analyzers.

Flexible Customization: Offers flexible customization options for reagent specifications.

ISO Certifications: Company holds ISO9001:2015 and ISO13485 certifications for quality assurance.

100% Quality Inspection: All finished products undergo 100% visual and functional inspection.

Rapid Lead Time: Average lead time is within 15 workdays for both peak and off-peak seasons.

OEM Service Available: Original Equipment Manufacturer services are available for partners.

Traceable Raw Materials: Full traceability system is implemented for all raw materials used.

Experienced Manufacturer: Established in 2004 with 20 years of export experience and 16 R&D engineers.

Company profile

Importers and ExportersYears of Export Experience

Zhejiang Xinke Medical Technology Co., Ltd.

Zhejiang, China

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: OEM Service Available CertifiedCustomization Options: Flexible customization CertifiedExport Year: 20 Years CertifiedNearest Port: Ningbo PortAverage Response Time: ≤2.83h

AI-Powered supplier vetting

SummaryThe supplier operates in the clinical in vitro diagnostic reagent field and reports ten years of ISO9001 and ISO13485 quality-system certification. It offers flexible customization, has OEM experience with well-known brands, possesses self-managed import/export rights, and has exported for 20 years, with exports representing 51%–70% of total sales. Quality inspection procedures are documented and consistently followed, while stated lead times are within 15 working days in both peak and off-season. However, the supplier reports no inventory, overseas warehouse, overseas showroom, overseas agents or branches, offline trade-show participation, ODM service, SDK, recent new-product development, ERP, OA, CRM, SAP, or broader digitalization initiatives. Financial information is inconsistent or insufficiently interpretable in the provided records, so financial credibility cannot be determined.

Supplier typeThe supplier identifies itself as a company in the clinical in vitro diagnostic reagent field and has self-managed import/export rights with 20 years of export experience. This supports classification as an export-capable manufacturer or supplier in the medical in vitro diagnostics sector.

CertificationsThe company states that it has maintained ISO9001 and ISO13485 quality-system certifications for ten years. These explicitly documented certifications support a positive assessment of its quality-system credentials.

R&D capabilityThe supplier reports no new products in the past year, no ODM service, no available SDK, and no current enterprise digitalization or technical-transformation plan. These explicit limitations indicate weak demonstrated innovation capability.

Customization capabilityThe supplier explicitly provides flexible customization through both its R&D and design-service capabilities. This directly supports a positive assessment of customization capability, although ODM service is not offered.

Client casesThe supplier states that it provides OEM services for well-known brands, which is evidence of relevant customer experience. No specific brand names, project details, or verifiable case descriptions are provided, so the evidence is positive but limited.