Taiwan FDA registration aeb6abf275f397a5956ce5103ee4fe8e
"Anika" Medical Manual Surgical Instruments (Unsterilized)
TW: “愛尼卡”醫療用手動式手術器械 (未滅菌)
Taiwan·Risk Class 1·ENIKA CORPORATION·Registered Nov 20, 2006 – Nov 20, 2016CancelledRegistration details
- Analysis ID
- aeb6abf275f397a5956ce5103ee4fe8e
- Customs Code
- DHA04400535809
Company information
- Manufacturer
- ENIKA CORPORATION
- Manufacturer Country
- Pakistan
- Authorized Representative
- MIN SHIN INSTRUMENTS CO., LTD.
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 20, 2006
- Expiry Date
- Nov 20, 2016
- Cancellation Date
- Aug 13, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Anika" Medical Manual Surgical Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number aeb6abf275f397a5956ce5103ee4fe8e and manufactured by ENIKA CORPORATION. The authorized representative in Taiwan is MIN SHIN INSTRUMENTS CO., LTD..
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