Taiwan FDA registration ee8bdeb6bc6b0218915bee2b8856205b
"Vella" IOL guide (sterilization)
TW: “威朗” 人工水晶體導引器 (滅菌)
Taiwan·Risk Class 1·VALEANT MED Sp. z o.o.·Registered Jul 24, 2017 – Jul 24, 2022CancelledRegistration details
- Analysis ID
- ee8bdeb6bc6b0218915bee2b8856205b
- Customs Code
- DHA09401810201
Company information
- Manufacturer
- VALEANT MED Sp. z o.o.
- Manufacturer Country
- Poland
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
Product details
- Intended Use
- Limited to the first level identification range of "Intraocular Lens Guide (M.4300)" under the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4300 Artificial crystal body inducer
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jul 24, 2017
- Expiry Date
- Jul 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 "Vella" IOL guide (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ee8bdeb6bc6b0218915bee2b8856205b and manufactured by VALEANT MED Sp. z o.o.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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