Taiwan FDA registration 9e9ee9cfbb6ee1c190dd83a39d28c890
"Sindis" femur reconstruction intramedullary nail
TW: “信迪思”股骨重建髓內釘
Taiwan·Risk Class 2·SYNTHES GMBH;; Jabil Switzerland Manufacturing GmbH·Registered Mar 26, 2020 – Mar 26, 2030ActiveRegistration details
- Analysis ID
- 9e9ee9cfbb6ee1c190dd83a39d28c890
- Customs Code
- DHA05603341400
Company information
- Manufacturer Country
- Switzerland
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL 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.3020 骨髓內固定桿
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Mar 26, 2020
- Expiry Date
- Mar 26, 2030
About this record
Access comprehensive regulatory information for "Sindis" femur reconstruction intramedullary nail in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9e9ee9cfbb6ee1c190dd83a39d28c890 and manufactured by SYNTHES GMBH;; Jabil Switzerland Manufacturing GmbH. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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