Taiwan FDA registration 41d84f7e934f0f43e99f6aa02334d41e
"Willunme" Bayerkeni artificial vitreous
TW: “威倫美” 拜耳克尼人工玻璃體
Taiwan·Risk Class 3·VALEANT MED Sp. z o.o.·Registered Jan 16, 2012 – Jan 16, 2022CancelledRegistration details
- Analysis ID
- 41d84f7e934f0f43e99f6aa02334d41e
- Customs Code
- DHA00602322906
Company information
- Manufacturer
- VALEANT MED Sp. z o.o.
- Manufacturer Country
- Poland
- Authorized Representative
- CHIU HO MEDICAL SYSTEM CO., LTD.
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
- Jan 16, 2012
- Expiry Date
- Jan 16, 2022
- Cancellation Date
- Jan 03, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Willunme" Bayerkeni 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 41d84f7e934f0f43e99f6aa02334d41e and manufactured by VALEANT MED Sp. z o.o.. The authorized representative in Taiwan is CHIU HO MEDICAL SYSTEM CO., LTD..
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