Taiwan FDA registration 2e54598555e0a0c57c428c6b1a813bb0
"Sindis" Dormao medial distal femoral plate
TW: “信迪思”多茂內側遠端股骨骨板
Taiwan·Risk Class 2·SYNTHES GMBH;; Jabil Switzerland Manufacturing GmbH·Registered Aug 18, 2022 – Aug 18, 2027ActiveRegistration details
- Analysis ID
- 2e54598555e0a0c57c428c6b1a813bb0
- Customs Code
- DHA05603574701
Company information
- Manufacturer Country
- Switzerland
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3040 平滑或螺紋之金屬類骨固定物;; N.3030 單一或多重之金屬類骨固定裝置及附件
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Aug 18, 2022
- Expiry Date
- Aug 18, 2027
About this record
Access comprehensive regulatory information for "Sindis" Dormao medial distal femoral plate in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2e54598555e0a0c57c428c6b1a813bb0 and manufactured by SYNTHES GMBH;; Jabil Switzerland Manufacturing GmbH. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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