How do you ensure product quality?

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

What is your export experience?

We have been exporting for 20 years and serve markets in Europe, Southeast Asia, Middle East, and Africa.

Aia-Pack Analyzer Tosoh Serie Diluent Concentrate Immunoassay Buffer

Name: Aia-Pack Analyzer Tosoh Serie Diluent Concentrate Immunoassay Buffer
Brand: Zhejiang Xinke Medical Technology Co., Ltd.
SKU: 1952409551

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

Probe Cleaner

Model NO.

JXK-177

Volume

250ml

OEM

Yes

Brand

Xinke

Transport Package

Carton

Specification

100ml*4

Trademark

xinke

Origin

China

HS Code

3822190090

Production Capacity

500000/Ctns

Key features

OEM Service Available: Flexible customization options provided for tailored product needs.

100% Finished Product Inspection: All items undergo visual and functional inspection before shipment.

ISO9001:2015 Certified: Manufacturing process meets international quality management standards.

Fast Lead Time: Production completed within 15 workdays for both peak and off-peak seasons.

Traceable Raw Materials: Full traceability system ensures quality and safety of all raw materials.

Experienced Manufacturer: Over 20 years of export experience with 16 R&D engineers and 122 employees.

Flexible MOQ: Minimum order quantity starts from just 1 piece for customer convenience.

Diverse Payment Options: Supports LC, T/T, D/P, PayPal, Western Union, and small-amount payments.

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: ≤3.06h

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.