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"Bury" irregular antibody detection kit - Taiwan Registration 6949a7bf022d9d2779943d5d20f2e46e

Access comprehensive regulatory information for "Bury" irregular antibody detection kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6949a7bf022d9d2779943d5d20f2e46e 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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6949a7bf022d9d2779943d5d20f2e46e
Registration Details
Taiwan FDA Registration: 6949a7bf022d9d2779943d5d20f2e46e
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Device Details

"Bury" irregular antibody detection kit
TW: โ€œไผฏ็‘žโ€ ไธ่ฆๅ‰‡ๆŠ—้ซ”ๆชขๆธฌ่ฉฆๅŠ‘็ต„
Risk Class 2

Registration Details

6949a7bf022d9d2779943d5d20f2e46e

DHA05603524207

Company Information

Product Details

Detection reagents for antibodies to red blood cell irregularities.

B Hematology, pathology, and genetics

B.9300 Coomb's Automatic Testing System

Input;; QMS/QSD

Dates and Status

Apr 25, 2022

Apr 25, 2027