Taiwan FDA registration 9e5d7be49050bbef95aacddb45a37e39
"Stryker" third generation titanium alloy locking bone plate system
TW: “史賽克”第三代鈦合金鎖定骨板系統
Taiwan·Risk Class 2·Stryker GmbH·Registered Aug 12, 2016 – Aug 12, 2026ActiveRegistration details
- Analysis ID
- 9e5d7be49050bbef95aacddb45a37e39
- Customs Code
- DHA05602872905
Company information
- Manufacturer
- Stryker GmbH
- Manufacturer Country
- Switzerland
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
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.3030 Single or multiple metallic bone fixation devices and accessories
- Import Information
- import
Dates and status
- Registration Date
- Aug 12, 2016
- Expiry Date
- Aug 12, 2026
About this record
Access comprehensive regulatory information for "Stryker" third generation titanium alloy locking bone plate system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9e5d7be49050bbef95aacddb45a37e39 and manufactured by Stryker GmbH. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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