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Venice PU OK繃 (未滅菌) - Taiwan Registration 18cdd29db98def9511f0b7575f19fbb2

Access comprehensive regulatory information for Venice PU OK繃 (未滅菌) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 18cdd29db98def9511f0b7575f19fbb2 and manufactured by VENICE LABORATORIES CO., LTD.. The authorized representative in Taiwan is VENICE LABORATORIES 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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18cdd29db98def9511f0b7575f19fbb2
Registration Details
Taiwan FDA Registration: 18cdd29db98def9511f0b7575f19fbb2
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Device Details

Venice PU OK繃 (未滅菌)
Risk Class 1

Registration Details

18cdd29db98def9511f0b7575f19fbb2

DHY04300044300

Company Information

Taiwan, Province of China

Product Details

It is used to cover and protect the wound and to join the skin wound.

J General hospital and personal use equipment

J.5240 Adhesive tapes and adhesive bandages for medical use

Domestic

Dates and Status

Oct 24, 2005

Oct 24, 2025