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"Immulab" Rapid Antibody Medium LISS Additive(Non-Sterile) - Taiwan Registration 2610711bbae0a7b86d3efbe8880449be

Access comprehensive regulatory information for "Immulab" Rapid Antibody Medium LISS Additive(Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2610711bbae0a7b86d3efbe8880449be and manufactured by IMMULAB PTY LTD. The authorized representative in Taiwan is GLORY BIOSCIENCE CO., LTD..

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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2610711bbae0a7b86d3efbe8880449be
Registration Details
Taiwan FDA Registration: 2610711bbae0a7b86d3efbe8880449be
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Device Details

"Immulab" Rapid Antibody Medium LISS Additive(Non-Sterile)
TW: "ไพๅ…็พ…" ไฝŽ้›ขๅญๆทปๅŠ ๆถฒ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

2610711bbae0a7b86d3efbe8880449be

Ministry of Health Medical Device Import No. 021636

DHA09402163609

Company Information

Australia

Product Details

Limited to the first level identification range of intensive medium (B.9600) for in vitro diagnosis of medical device management methods.

B Hematology and pathology devices

B9600 Fortified medium for in vitro diagnostics

Imported from abroad

Dates and Status

Jun 15, 2020

Jun 15, 2025