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DirectCHECK Whole Blood Control - Taiwan Registration 670170a433c3a65761a4ff7f8170874f

Access comprehensive regulatory information for DirectCHECK Whole Blood Control in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 670170a433c3a65761a4ff7f8170874f and manufactured by Accriva Diagnostics Inc.. The authorized representative in Taiwan is Werfen Taiwan Limited.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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670170a433c3a65761a4ff7f8170874f
Registration Details
Taiwan FDA Registration: 670170a433c3a65761a4ff7f8170874f
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Device Details

DirectCHECK Whole Blood Control
TW: ๅพท็ขบ ๅ…จ่ก€ๅ“็ฎกๆถฒ
Risk Class 2
MD

Registration Details

670170a433c3a65761a4ff7f8170874f

Ministry of Health Medical Device Import No. 030087

DHA05603008709

Company Information

United States

Product Details

Quality control materials for monitoring Hammock microcoagulation time analyzers.

A Clinical chemistry and clinical toxicology

A1660 Quality Control Materials (Analytical and Non-Analytical)

Imported from abroad

Dates and Status

Oct 24, 2017

Oct 24, 2027