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Venice PE OK 繃 (未滅菌) - Taiwan Registration 6504d6387313102579d9a3f490946562

Access comprehensive regulatory information for Venice PE 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 6504d6387313102579d9a3f490946562 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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6504d6387313102579d9a3f490946562
Registration Details
Taiwan FDA Registration: 6504d6387313102579d9a3f490946562
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Device Details

Venice PE OK 繃 (未滅菌)
Risk Class 1

Registration Details

6504d6387313102579d9a3f490946562

DHY04300044501

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