Taiwan FDA registration 0c09fd251eedfc599f15815982d1047e
“Valeant Med” FOCUSforce ULTRAflex Spheric Intraocular Lens
TW: “威朗”博科視單片式球面人工水晶體
Taiwan·Risk Class 3·MD·VALEANT MED Sp. z o.o.·Registered Jul 19, 2017 – Jul 19, 2022ExpiredRegistration details
- Analysis ID
- 0c09fd251eedfc599f15815982d1047e
- License Form
- Ministry of Health Medical Device Import No. 029976
- Customs Code
- DHA05602997601
Company information
- Manufacturer
- VALEANT MED Sp. z o.o.
- Manufacturer Country
- Poland
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M3600 intraocular lens
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 19, 2017
- Expiry Date
- Jul 19, 2022
About this record
Access comprehensive regulatory information for “Valeant Med” FOCUSforce ULTRAflex Spheric Intraocular Lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 0c09fd251eedfc599f15815982d1047e and manufactured by VALEANT MED Sp. z o.o.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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