Taiwan FDA registration 4c0b4c34e749d4dcf0ad4c64fe3ef9d6
"Stryker" Scrobio classic tibial inner pad
TW: “史賽克”斯高比歐經典脛骨內墊
Taiwan·Risk Class 2·STRYKER IRELAND LIMITED·Registered Apr 24, 2012 – Apr 24, 2022CancelledRegistration details
- Analysis ID
- 4c0b4c34e749d4dcf0ad4c64fe3ef9d6
- Customs Code
- DHA00602354006
Company information
- Manufacturer
- STRYKER IRELAND LIMITED
- Manufacturer Country
- Ireland
- 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.3565 Knee jointsFemoral metals/polymersPorous coatings of cementless cement
- Import Information
- import
Dates and status
- Registration Date
- Apr 24, 2012
- Expiry Date
- Apr 24, 2022
- Cancellation Date
- May 30, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Stryker" Scrobio classic 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 4c0b4c34e749d4dcf0ad4c64fe3ef9d6 and manufactured by STRYKER IRELAND LIMITED. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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