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Venice 伸縮OK繃 (未滅菌) - Taiwan Registration 1eb4d0373cbe0a52293be62345540338

Access comprehensive regulatory information for Venice 伸縮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 1eb4d0373cbe0a52293be62345540338 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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1eb4d0373cbe0a52293be62345540338
Registration Details
Taiwan FDA Registration: 1eb4d0373cbe0a52293be62345540338
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Device Details

Venice 伸縮OK繃 (未滅菌)
Risk Class 1

Registration Details

1eb4d0373cbe0a52293be62345540338

DHY04300056001

Company Information

Taiwan, Province of China

Product Details

It is used to cover and protect the wound and to join the skin wound. Not suitable for severe burns (grade 3).

J General hospital and personal use equipment

J.5240 Adhesive tapes and adhesive bandages for medical use

Domestic

Dates and Status

Oct 30, 2005

Oct 30, 2025