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Berry External Quality Assurance Program for HIV/Hepatitis (Unsterilized) - Taiwan Registration 8769327027955fccfd93ccaf5d22b218

Access comprehensive regulatory information for Berry External Quality Assurance Program for HIV/Hepatitis (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8769327027955fccfd93ccaf5d22b218 and manufactured by BIO-RAD LABORATORIES INC.. The authorized representative in Taiwan is Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.).

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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8769327027955fccfd93ccaf5d22b218
Registration Details
Taiwan FDA Registration: 8769327027955fccfd93ccaf5d22b218
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Device Details

Berry External Quality Assurance Program for HIV/Hepatitis (Unsterilized)
TW: "ไผฏ็‘ž" ๆ„›ๆป‹็—…ๆฏ’/่‚็‚Žๅค–้ƒจๅ“ไฟ่จˆ็•ซ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

8769327027955fccfd93ccaf5d22b218

DHA09401668706

Company Information

United States

Product Details

Limited to the classification and grading management of medical equipment, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.

A Clinical chemistry and clinical toxicology

A.1660 Quality control materials (analytical and non-analytical)

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Jun 23, 2016

Jun 23, 2026