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"Lemen" debridement gel (sterilized) - Taiwan Registration 86c668f1bcf99aa26c8d37efd0a76b28

Access comprehensive regulatory information for "Lemen" 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 86c668f1bcf99aa26c8d37efd0a76b28 and manufactured by LOHMANN & RAUSCHER INTERNATIONAL GMBH & CO. KG. The authorized representative in Taiwan is HOREB ENTERPRISE 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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86c668f1bcf99aa26c8d37efd0a76b28
Registration Details
Taiwan FDA Registration: 86c668f1bcf99aa26c8d37efd0a76b28
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Device Details

"Lemen" debridement gel (sterilized)
TW: ใ€ๆจ‚้–€ใ€žๆธ…ๅ‰ตๅ‡่† (ๆป…่Œ)
Risk Class 1

Registration Details

86c668f1bcf99aa26c8d37efd0a76b28

DHA04401136008

Company Information

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

Input;; QMS/QSD

Dates and Status

Feb 10, 2012

Feb 10, 2027