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Dirui Biochemistry Dr Acid Detergent Cleaning Solution Reagents for Dirui Ivd Analyzer CS Series

Name: Dirui Biochemistry Dr Acid Detergent Cleaning Solution Reagents for Dirui Ivd Analyzer CS Series
Brand: Zhejiang Xinke Medical Technology Co., Ltd.
SKU: 2164776425

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

Compatible Models

Dirui CS Series

Transport Package

Carton

Specification

Trademark

xinke

Origin

China

HS Code

3822190090

Production Capacity

500000/Ctns

Key features

100% Original Compatibility: Reagents are 100% compatible with Dirui CS Series analyzers including CS-6400, 1200, 800B, 600B, 400B, 300B, CS-T300, and T300B.

OEM Service Available: We offer flexible OEM customization services to meet your specific brand and model requirements.

Sample Testing Support: Samples are offered for comparison testing to ensure product quality and compatibility before bulk orders.

Strict Quality Assurance: Every batch undergoes quality testing and final inspection before shipping, with reports included.

Professional Manufacturer: Established in 2004, Zhejiang Xinke Medical Technology Co., Ltd. is a professional IVD reagent manufacturer.

Multiple Certifications: Products hold ISO9001, ISO13485, CE, and MSDS certifications ensuring international standards compliance.

Low Minimum Order Quantity: Minimum Order Quantity is just 1 piece, allowing for flexible purchasing and trial orders.

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

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: ≤2.76h

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.