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Coloplast Wound Debridement Gel (Sterilized) - Taiwan Registration c1293311279f27729d3bef4bc8501d1b

Access comprehensive regulatory information for Coloplast Wound Debridement Gel (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c1293311279f27729d3bef4bc8501d1b and manufactured by COLOPLAST A/S;; Curida AS. The authorized representative in Taiwan is COLOPLAST TAIWAN 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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c1293311279f27729d3bef4bc8501d1b
Registration Details
Taiwan FDA Registration: c1293311279f27729d3bef4bc8501d1b
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Device Details

Coloplast Wound Debridement Gel (Sterilized)
TW: ใ€ๅบทๆจ‚ไฟใ€žๅ‚ทๅฃๆธ…ๅ‰ตๅ‡่†  (ๆป…่Œ)
Risk Class 1

Registration Details

c1293311279f27729d3bef4bc8501d1b

DHA04401290503

Company Information

Norway;;Denmark

Product Details

Limited to the first level of classification and grading management of medical equipment "Waterborne Wound and Burn Covering (I.4022)".

I General, Plastic Surgery and Dermatology

I.4022 Water-based wounds and burn covers

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Apr 12, 2013

Apr 12, 2028