Taiwan FDA registration cbdf3463b8657db1c19cee02453e5555
"Asukole" intranasal fixation splint (sterilized)
TW: "阿碩柯爾"鼻腔內固定夾板 (滅菌)
Taiwan·Risk Class 1·ARTHROCARE CORPORATION·Registered Nov 03, 2015 – Nov 03, 2025ExpiredRegistration details
- Analysis ID
- cbdf3463b8657db1c19cee02453e5555
- Customs Code
- DHA09401580507
Company information
- Manufacturer
- ARTHROCARE CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.)
Product details
- Intended Use
- It is limited to the first level of identification of the "Nasal Fixation (G.4780)" of the Administrative Measures for the Classification and Classification of Medical Devices.
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4780 Nasal fixations
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Nov 03, 2015
- Expiry Date
- Nov 03, 2025
About this record
Access comprehensive regulatory information for "Asukole" intranasal fixation splint (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cbdf3463b8657db1c19cee02453e5555 and manufactured by ARTHROCARE CORPORATION. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).
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