Single Use Peripheral Blood Collection Safety Blood Lancets Care Kit

Name: Single Use Peripheral Blood Collection Safety Blood Lancets Care Kit
Brand: Maide Medical Devices(Wenzhou)Co., Ltd.
SKU: 1979237131

Zhejiang, ChinaMaide Medical Devices(Wenzhou)Co., Ltd.

US$0.085

5,000 Pieces

Sample price:US$0.12/piece.Request sample

Product profile

Customization

Available

Type

Disposable Peripheral Blood Collection Care Kit

Material

ABS, Stainless Steel 304

Model NO.

D 23G PA II+ TW

Ethylene Oxide Sterilization

Quality Guarantee Period

2 Years

Group

All

Logo Printing

OEM Available

MOQ

5000PCS

OEM

Available

Certificates

CE, FDA510K, ISO13485, ISO9001

Model

Gauge

23G

Depth

2.2mm

Color

Green

Application

Disposable Peripheral Blood Collection

Transport Package

Carton

Specification

23G

Trademark

OEM service

Origin

China

HS Code

90183900

Production Capacity

10000000

Company profile

Importers and ExportersHigh Repeat Buyers Choice

Maide Medical Devices(Wenzhou)Co., Ltd.

Zhejiang, China

CertifiedBusiness Type: Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Customization from Samples, Customization from Designs CertifiedExport Year: 5 Years CertifiedNearest Port: Ningbo PortAverage Response Time: ≤5.99h

AI-Powered supplier vetting

SummaryMaide Medical Devices(Wenzhou)Co., Ltd. is identified as a Chinese trading company established in 2020, with two employees and a Zhejiang address. The available records associate it with lancets and also report a Shandong factory location, six to ten quality-control staff, and stated safety-lancet output, but the relationship between the trading entity and factory information is not clarified. The supplier offers broad customization services and has in-stock capability. However, only one R&D engineer is reported, no new products were launched in the previous year, no SDK is available, and documented complaint-handling and corrective/preventive-action procedures are absent. Certification or successful audit evidence is insufficient: an audit record exists, but its evaluation result is recorded as 0 and the report validity period has expired. Financial records are referenced for 2021–2023, but no financial figures or assessment results are provided. Customer cases are not identified.

CertificationsAn audit by TUVRHEINLAND is recorded, but the audit evaluation result is listed as 0, and the SGS report validity ended on 2025-09-28. No valid certification or successful certification outcome is explicitly provided.

After-Sales capabilityThe supplier has in-stock service capability, but it has no overseas warehouse or showroom. More importantly, no written procedures or records were provided for effective customer complaint handling or corrective and preventive actions, indicating a documented service-process deficiency.

R&D capabilityThe supplier reports one R&D engineer, no new products launched in the previous year, and no available SDK. These explicit indicators show limited demonstrated innovation capability.

Customization capabilityThe supplier explicitly offers customization from samples, customization from designs, full customization, minor customization, and flexible customization. This is direct evidence of broad customization service capability.