Taiwan FDA registration ecd4ca5301c57c896eee891e1011db4e
"Stryker" artificial femur
TW: "史賽克" 人工股骨
Taiwan·Risk Class 2·STRYKER IRELAND LIMITED·Registered Jun 25, 1999 – Aug 02, 2021CancelledRegistration details
- Analysis ID
- ecd4ca5301c57c896eee891e1011db4e
- Customs Code
- DHA00600921500
Company information
- Manufacturer
- STRYKER IRELAND LIMITED
- Manufacturer Country
- Ireland
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- Product Type (Level 1)
- 0399 Other artificial function substitutes
- Import Information
- import
Dates and status
- Registration Date
- Jun 25, 1999
- Expiry Date
- Aug 02, 2021
- Cancellation Date
- Sep 18, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Stryker" artificial femur in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ecd4ca5301c57c896eee891e1011db4e and manufactured by STRYKER IRELAND LIMITED. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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