Taiwan FDA registration 2b717c64cee0a9abda084eb0a4900ba8
Defusol Debridement Dressing (Sterilized)
TW: 德膚舒清創敷料 (滅菌)
Registration details
- Analysis ID
- 2b717c64cee0a9abda084eb0a4900ba8
- Customs Code
- DHA09401843502
Company information
- Manufacturer
- LOHMANN & RAUSCHER INTERNATIONAL GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- SEQPRO, INC.
Product details
- Intended Use
- Limited to the first level of identification scope of "external use of non-absorbent gauze or sponge balls (I.4014)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4014 Non-absorbent cloth or sea balls are used externally
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Oct 20, 2017
- Expiry Date
- Oct 20, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Defusol Debridement Dressing (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2b717c64cee0a9abda084eb0a4900ba8 and manufactured by LOHMANN & RAUSCHER INTERNATIONAL GMBH & CO. KG. The authorized representative in Taiwan is SEQPRO, INC..
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.
Free DatabasePowered by Pure Global AI89,000+ Devices