Taiwan FDA registration 31be0a2195d8ae5551249df755f4aa4a
“Croma” Eyefill DC Viscoelastic Solution
TW: “寇瑪” 艾飛爾分散內聚雙重人工玻璃體
Taiwan·Risk Class 3·MD·VALEANT MED Sp. z o.o.·Registered Nov 04, 2013 – Nov 04, 2023ExpiredRegistration details
- Analysis ID
- 31be0a2195d8ae5551249df755f4aa4a
- License Form
- Ministry of Health Medical Device Import No. 025574
- Customs Code
- DHA05602557400
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)
- M4275 Liquid for intraocular filling
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 04, 2013
- Expiry Date
- Nov 04, 2023
About this record
Access comprehensive regulatory information for “Croma” Eyefill DC Viscoelastic Solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 31be0a2195d8ae5551249df755f4aa4a and manufactured by VALEANT MED Sp. z o.o.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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