Taiwan FDA registration 815743fb8eea65991a9365c29a2fd228
"Koma" Effel artificial vitreous
TW: “寇瑪”艾飛爾人工玻璃體
Registration details
- Analysis ID
- 815743fb8eea65991a9365c29a2fd228
- Customs Code
- DHA00602255300
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 Ophthalmology
- Product Type (Level 2)
- M.4275 眼內充填用液體
- Import Information
- import
Dates and status
- Registration Date
- Jun 20, 2011
- Expiry Date
- Jun 20, 2026
About this record
Access comprehensive regulatory information for "Koma" Effel artificial vitreous in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 815743fb8eea65991a9365c29a2fd228 and manufactured by VALEANT MED Sp. z o.o.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices