Taiwan FDA registration d450eb3f16ea3f3f5a19695856eb1198
"Weishi" general surgery manual instrument (unsterilized)
TW: “威士”一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·WISE MEDICAL CO·Registered Nov 04, 2011 – Nov 04, 2016CancelledRegistration details
- Analysis ID
- d450eb3f16ea3f3f5a19695856eb1198
- Customs Code
- DHA04401102201
Company information
- Manufacturer
- WISE MEDICAL CO
- Manufacturer Country
- Pakistan
- Authorized Representative
- HOME YOUR CORPORATION
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- import
Dates and status
- Registration Date
- Nov 04, 2011
- Expiry Date
- Nov 04, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Weishi" general surgery manual instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d450eb3f16ea3f3f5a19695856eb1198 and manufactured by WISE MEDICAL CO. The authorized representative in Taiwan is HOME YOUR CORPORATION.
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