Does the manufacturer offer custom logo printing?

Yes, logo printing is available as a customization option.

What is the lead time for orders?

Peak season lead time is one month, while off-season lead time is within 15 workdays.

What payment terms are accepted?

Accepted terms include LC, T/T, D/P, PayPal, and Western Union.

CE Approved EDTA K2 EDTA K3 Disposable Blood Collection Tube for Blood Routine

Name: CE Approved EDTA K2 EDTA K3 Disposable Blood Collection Tube for Blood Routine
Brand: Changsha Renji Medical Equipments Co., Ltd.
SKU: 2044540145

Hunan, ChinaChangsha Renji Medical Equipments Co., Ltd.

US$0.04

10,000-99,999 Pieces

US$0.03

100,000+ Pieces

Sample price:US$0.00/piece.Request sample

Product profile

Customization

Available

Type

Vacuum Blood Tube & Blood Bag

Material

Plastic

Ethylene Oxide Sterilization

Quality Guarantee Period

Two Years

Group

Adult

Logo Printing

With Logo Printing

Model No.

EDTA K2 K3

Cap Color

Lavender

Cap Material

Sample Type

Blood

Centrifuge

No Centrifugation Performed

Capacity

2ml, 3ml, 4ml, 5ml, 6ml, 7ml, 8ml, 9ml, 10ml

Clotting Time

Blood Will Not Freeze

Transport Package

Carton

Specification

2ml, 3ml, 4ml, 5ml, 6ml, 7ml, 8ml, 9ml, 10ml

Trademark

Renji

Origin

China

HS Code

9018390000

Production Capacity

500000/Day

Key features

CE Approved Quality: Certified for safety and compliance with European medical standards.

Ethylene Oxide Sterilization: Ensures complete sterility for safe blood collection procedures.

Comprehensive Blood Protection: EDTA K2/K3 preserves blood cell form and volume, protecting platelets.

Direct Sampling Compatibility: Compatible with direct sampling analyzers without opening the tube.

Two-Year Shelf Life: Guaranteed stability and quality for 24 months from manufacture.

Multiple Capacity Options: Available in 2ml, 3ml, 4ml, 5ml, 6ml, 7ml, 8ml, 9ml, and 10ml sizes.

Custom Logo Printing: Service available for adding custom branding to the tubes.

Wide Clinical Application: Ideal for clinical hematology and various blood cell test instruments.

Company profile

Self-brandedStandardized quality controlR&D CapabilitiesManagement Certification

Changsha Renji Medical Equipments Co., Ltd.

Hunan, China

Business Type: Manufacturer/Factory, Trading CompanyExport Year: 2020-10-01Nearest Port: guangzhou, shenzhen, shanghaiAverage Response Time: ≤6.12hTerms of Payment: LC, T/T, D/P, etc.International Commercial Terms(Incoterms): FOB, CFR, CIF, FCA, EXW

AI-Powered supplier vetting

SummaryThe supplier is identified as a manufacturing factory producing sanitary materials, medical supplies, medical devices, disinfection products, and sanitary equipment. It reports customization from samples, designs, and full specifications, with two production lines and export markets spanning multiple regions. Quality and service procedures are documented, and the supplier states that it holds or has products approved by CE, SGS, ISO13485, NMPA, and ISO9001:2015-related certification. It also reports OEM service for known brands and experience exporting to more than 50 countries. However, no SDK is available, and the supplier lacks in-stock service, overseas warehouse, overseas showroom, and a valid manufacturing-capacity contract with affiliated subcontractors. Financial information is represented only by years rather than usable performance figures, so financial credibility cannot be determined.

Supplier typeThe supplier is explicitly identified as a factory, with a business scope covering manufacturing of sanitary materials, medical supplies, medical devices, disinfection products, and sanitary equipment. Its associated companies are classified in manufacturing, supporting a direct manufacturing-supplier profile.

CertificationsThe supplier reports an ISO9001:2015 certificate and states that its products have been approved by CE, SGS, ISO13485, and NMPA, among others. These stated certifications and approvals provide explicit evidence of certification coverage, although the slices do not provide certificate numbers, validity dates, or scope details.

After-Sales capabilityThe supplier reports written and followed procedures for service-capability assessment, corrective and preventive actions, and customer complaint handling. This is explicit evidence of a documented after-sales and complaint-management system.

R&D capabilityThe supplier explicitly reports no available SDK, which limits evidence of software-development or integration capability. Although it emphasizes product certifications and customer-oriented management, the slices do not establish broader research, product-development, or innovation performance.

Production capacityThe supplier operates two production lines, reports peak-season fulfillment of one month and off-peak lead time within 15 working days, and has export access through major Chinese ports. However, it reports no in-stock capacity and no valid manufacturing-capacity contract with affiliated subcontractors, creating explicit operational limitations despite its stated factory capacity.

Customization capabilityThe supplier explicitly offers customization from samples, designs, and full customization, and also reports OEM service for known brands. These capabilities directly support customized and OEM manufacturing requirements.

Client casesThe supplier states that it provides OEM services for known brands and has export experience involving more than 50 countries. These statements indicate brand-related and international customer experience, but no specific customer names, project details, or independently verifiable cases are provided.