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DiaClon Anti-A - Taiwan Registration 048f4ad28833f7d3d7b4de441c057ed9

Access comprehensive regulatory information for DiaClon Anti-A in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 048f4ad28833f7d3d7b4de441c057ed9 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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048f4ad28833f7d3d7b4de441c057ed9
Registration Details
Taiwan FDA Registration: 048f4ad28833f7d3d7b4de441c057ed9
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Device Details

DiaClon Anti-A
TW: โ€œไผฏ็‘žโ€ ๅ–ฎๆ ชๆŠ—้ซ”ๆŠ—Aๅž‹้‘‘ๅฎš่ฉฆๅŠ‘
Risk Class 3
MD

Registration Details

048f4ad28833f7d3d7b4de441c057ed9

Ministry of Health Medical Device Import No. 032169

DHA05603216908

Company Information

Switzerland

Product Details

This product contains a single strain of IgM antibody, which can be used for classification of blood group A by slide or test tube method.

B Hematology and pathology devices

B4020 Analyze specific reagents

Imported from abroad

Dates and Status

Feb 13, 2019

Feb 13, 2029