Taiwan FDA registration 5736069967117cb76c0e6057f92b8230
"Stryker" Scroby Ou tibial inner pad
TW: "史賽克" 斯高比歐脛骨內墊
Taiwan·Risk Class 2·STRYKER IRELAND LIMITED·Registered May 23, 2002 – May 23, 2017CancelledRegistration details
- Analysis ID
- 5736069967117cb76c0e6057f92b8230
- Customs Code
- DHA00600993406
Company information
- Manufacturer
- STRYKER IRELAND LIMITED
- Manufacturer Country
- Ireland
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- Intended Use
- Vacuum.
- Product Type (Level 1)
- N Orthopedics
- Import Information
- import
Dates and status
- Registration Date
- May 23, 2002
- Expiry Date
- May 23, 2017
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Stryker" Scroby Ou tibial inner pad in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5736069967117cb76c0e6057f92b8230 and manufactured by STRYKER IRELAND LIMITED. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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