Taiwan FDA registration d97bd667eeec751f97e5317f856be0ad
"Bivier" Manual Eye Surgery Instruments (Sterilized)
TW: "畢威艾" 手動式眼科手術器械 (滅菌)
Taiwan·Risk Class 1·BEAVER-VISITEC INTERNATIONAL, INC.·Registered Feb 24, 2017 – Feb 24, 2022CancelledRegistration details
- Analysis ID
- d97bd667eeec751f97e5317f856be0ad
- Customs Code
- DHA09401752501
Company information
- Manufacturer
- BEAVER-VISITEC INTERNATIONAL, INC.
- Manufacturer Country
- United States
- Authorized Representative
- CLINICO INC.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4350 手動式眼科手術器械
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Feb 24, 2017
- Expiry Date
- Feb 24, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bivier" Manual Eye Surgery Instruments (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d97bd667eeec751f97e5317f856be0ad and manufactured by BEAVER-VISITEC INTERNATIONAL, INC.. The authorized representative in Taiwan is CLINICO INC..
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