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HemosIL Q.F.A Thrombin (Bovine) - Taiwan Registration 51c3f1dfd44a3605ada068b2b7f28fad

Access comprehensive regulatory information for HemosIL Q.F.A Thrombin (Bovine) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 51c3f1dfd44a3605ada068b2b7f28fad and manufactured by INSTRUMENTATION LABORATORY CO.. The authorized representative in Taiwan is Werfen Taiwan Limited.

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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51c3f1dfd44a3605ada068b2b7f28fad
Registration Details
Taiwan FDA Registration: 51c3f1dfd44a3605ada068b2b7f28fad
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Device Details

HemosIL Q.F.A Thrombin (Bovine)
TW: ๅธŒๆ‘ฉ่ฅฟ็ˆพ็บ–็ถญ่›‹็™ฝๅŽŸ่ฉฆๅŠ‘
Risk Class 2
MD

Registration Details

51c3f1dfd44a3605ada068b2b7f28fad

Ministry of Health Medical Device Import No. 031725

DHA05603172507

Company Information

United States

Product Details

This product is paired with the IL Coagulation System of the Instrument Experimental Company, which uses the Clauss method to quantify the concentration of fibrinogen in human plasma with citric acidification.

B Hematology and pathology devices

B7875 Coagulation time test

Imported from abroad

Dates and Status

Oct 09, 2018

Oct 09, 2028