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“Lorne” Anti-e Monoclonal - Taiwan Registration 1fc64d0369a3d51951e684f1a0c0f717

Access comprehensive regulatory information for “Lorne” Anti-e Monoclonal in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1fc64d0369a3d51951e684f1a0c0f717 and manufactured by Lorne Laboratories 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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1fc64d0369a3d51951e684f1a0c0f717
Registration Details
Taiwan FDA Registration: 1fc64d0369a3d51951e684f1a0c0f717
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Device Details

“Lorne” Anti-e Monoclonal
TW: “羅倫” 單株抗體抗e血清試劑
Risk Class 2
MD

Registration Details

1fc64d0369a3d51951e684f1a0c0f717

Ministry of Health Medical Device Import No. 032013

DHA05603201303

Company Information

United Kingdom

Product Details

Appraisal e blood type fraction.

B Hematology and pathology devices

B4020 Analyze specific reagents

Imported from abroad

Dates and Status

Jan 08, 2019

Jan 08, 2029