Taiwan FDA registration d8ebefbae35280493951784d9b70ad09
"Stryker" cystoscopy
TW: “史賽克”膀胱鏡
Taiwan·Risk Class 2·STRYKER ENDOSCOPY·Registered Jun 08, 2009 – Jun 08, 2019CancelledRegistration details
- Analysis ID
- d8ebefbae35280493951784d9b70ad09
- Customs Code
- DHA00601989502
Company information
- Manufacturer
- STRYKER ENDOSCOPY
- Manufacturer Country
- United States
- 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)
- H Gastroenterology and urology
- Import Information
- import
Dates and status
- Registration Date
- Jun 08, 2009
- Expiry Date
- Jun 08, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Stryker" cystoscopy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d8ebefbae35280493951784d9b70ad09 and manufactured by STRYKER ENDOSCOPY. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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