Taiwan FDA registration 2725c19cf35303fd1ffe0235b88841c7
"Medtronic" Kaifeng expansion syringe
TW: “美敦力”凱豐擴張注射器
Taiwan·Risk Class 2·MEDTRONIC SOFAMOR DANEK USA, INC.·Registered Jul 01, 2016 – Jul 01, 2026ExpiredRegistration details
- Analysis ID
- 2725c19cf35303fd1ffe0235b88841c7
- Customs Code
- DHA05602867801
Company information
- Manufacturer
- MEDTRONIC SOFAMOR DANEK USA, INC.
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.9999 Miscellaneous
- Import Information
- import
Dates and status
- Registration Date
- Jul 01, 2016
- Expiry Date
- Jul 01, 2026
About this record
Access comprehensive regulatory information for "Medtronic" Kaifeng expansion syringe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2725c19cf35303fd1ffe0235b88841c7 and manufactured by MEDTRONIC SOFAMOR DANEK USA, INC.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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