Taiwan FDA registration 8e3cc108f89db43fd49ae5c4dd4e75dd
"Stryker" flexible cystoscopy
TW: “史賽克”軟式膀胱鏡
Taiwan·Risk Class 2·STRYKER ENDOSCOPY·Registered Apr 13, 2007 – Apr 13, 2017CancelledRegistration details
- Analysis ID
- 8e3cc108f89db43fd49ae5c4dd4e75dd
- Customs Code
- DHA00601801101
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
- Apr 13, 2007
- Expiry Date
- Apr 13, 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" flexible cystoscopy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8e3cc108f89db43fd49ae5c4dd4e75dd and manufactured by STRYKER ENDOSCOPY. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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