Is the product quality inspected?

Yes, 100% inspection including visual and functional checks is performed on finished products.

Where is the company located?

The company is located in Jinhua City, Zhejiang Province, China.

What is the shelf life or validity?

Specific shelf life details are not provided in the product description.

CD3700 Sheath ISO 13485

Name: Abbott Hematology Analyzer Reagent for CD3000/ CD3500 / CD3700 Sheath ISO 13485
Brand: Zhejiang Xinke Medical Technology Co., Ltd.
SKU: 2214262865

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

Product Name

Sheath

Model NO.

JXK-272

Application

Human

Certificate

CE ISO9001 ISO13485

Model

Abbott CD3000/ CD3500 / CD3700

Transport Package

Carton

Specification

20L

Trademark

Xinke

Origin

China

Key features

ISO 13485 Certified: Manufactured under ISO 13485 quality management system standards.

Flexible Customization: Offers flexible customization options for specific requirements.

OEM Service Available: OEM services are available for branded production needs.

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

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

Manufacturer Direct: Direct supply from manufacturer with 122 employees and 12,236 sqm plant area.

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

Global Shipping Terms: Supports CIF, CFR, FOB, and EXW terms for international trade.

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: ≤2.78h

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.