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"Burry" anti-Fyb serum reagent - Taiwan Registration f0137d0349a0105791379b5e63e0ce22

Access comprehensive regulatory information for "Burry" anti-Fyb serum reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f0137d0349a0105791379b5e63e0ce22 and manufactured by BIO-RAD MEDICAL DIAGNOSTICS GMBH. 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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f0137d0349a0105791379b5e63e0ce22
Registration Details
Taiwan FDA Registration: f0137d0349a0105791379b5e63e0ce22
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Device Details

"Burry" anti-Fyb serum reagent
TW: "ไผฏ็‘ž" ๆŠ—Fyb ่ก€ๆธ…่ฉฆๅŠ‘
Risk Class 2

Registration Details

f0137d0349a0105791379b5e63e0ce22

DHA05603569709

Company Information

Product Details

Indirect antiglobulin test to detect red blood cell antigen Fyb

B Hematology, pathology, and genetics

B.4020 Analysis of specific tests

Input;; QMS/QSD

Dates and Status

Aug 31, 2022

Aug 31, 2027