Taiwan FDA registration dcbae27360aeefb7ee4ef5484cfe0bf1
“ArthroCare” Coblator II System
TW: “阿碩柯爾”電刀系統
Taiwan·Risk Class 2·MD·SMITH & NEPHEW, INC. ENDOSCOPY DIVISION·Registered Nov 14, 2017 – Nov 14, 2027ActiveRegistration details
- Analysis ID
- dcbae27360aeefb7ee4ef5484cfe0bf1
- License Form
- Ministry of Health Medical Device Import No. 030396
- Customs Code
- DHA05603039609
Company information
- Manufacturer
- SMITH & NEPHEW, INC. ENDOSCOPY DIVISION
- Manufacturer Country
- United States
- 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)
- I4400 Electric knife for cutting and hemostasis and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 14, 2017
- Expiry Date
- Nov 14, 2027
About this record
Access comprehensive regulatory information for “ArthroCare” Coblator II System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dcbae27360aeefb7ee4ef5484cfe0bf1 and manufactured by SMITH & NEPHEW, INC. ENDOSCOPY DIVISION. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).
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