Taiwan FDA registration 00c2c6da71ce27a3ec9de7ea3ded0979
"Bausch & Len" Manual Eye Surgery Instruments (Unsterilized)
TW: "博士倫"手動式眼科手術器械(未滅菌)
Taiwan·Risk Class 1·BAUSCH & LOMB GMBH·Registered Sep 10, 2014 – Sep 10, 2019CancelledRegistration details
- Analysis ID
- 00c2c6da71ce27a3ec9de7ea3ded0979
- Customs Code
- DHA09401449309
Company information
- Manufacturer
- BAUSCH & LOMB GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
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
- Sep 10, 2014
- Expiry Date
- Sep 10, 2019
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Bausch & Len" Manual Eye Surgery 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 00c2c6da71ce27a3ec9de7ea3ded0979 and manufactured by BAUSCH & LOMB GMBH. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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