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DiaClon Anti-P1 - Taiwan Registration 308d6e98ab4697d9ede0d18f213ded83

Access comprehensive regulatory information for DiaClon Anti-P1 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 308d6e98ab4697d9ede0d18f213ded83 and manufactured by DIAMED 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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308d6e98ab4697d9ede0d18f213ded83
Registration Details
Taiwan FDA Registration: 308d6e98ab4697d9ede0d18f213ded83
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Device Details

DiaClon Anti-P1
TW: โ€œไผฏ็‘žโ€ ๅ–ฎๆ ชๆŠ—้ซ”ๆŠ—P1่ก€ๆธ…่ฉฆๅŠ‘
Risk Class 2
MD

Registration Details

308d6e98ab4697d9ede0d18f213ded83

Ministry of Health Medical Device Import No. 028435

DHA05602843501

Company Information

Switzerland

Product Details

An antigen-antibody reaction is used to detect the P1 antigen on red blood cells.

B Hematology and pathology devices

B4020 Analyze specific reagents

Imported from abroad

Dates and Status

May 31, 2016

May 31, 2026