Taiwan FDA registration 3ca26dcfd0fe790cdce3fd136bdb7b24
“Smith & Nephew” DURAFIBER Ag Silver Gelling Fibre Dressing
TW: “史耐輝”愛爾膚銀纖維抗菌敷料
Taiwan·Risk Class 2·MD·SMITH & NEPHEW MEDICAL LIMITED·Registered Feb 01, 2019 – Feb 01, 2024ExpiredRegistration details
- Analysis ID
- 3ca26dcfd0fe790cdce3fd136bdb7b24
- License Form
- Ministry of Health Medical Device Import No. 032236
- Customs Code
- DHA05603223600
Company information
- Manufacturer
- SMITH & NEPHEW MEDICAL LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4018 Hydrophilic trauma coverings
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 01, 2019
- Expiry Date
- Feb 01, 2024
About this record
Access comprehensive regulatory information for “Smith & Nephew” DURAFIBER Ag Silver Gelling Fibre Dressing in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3ca26dcfd0fe790cdce3fd136bdb7b24 and manufactured by SMITH & NEPHEW MEDICAL LIMITED. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).
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