Taiwan FDA registration d9028299ff4ab08770c94aba6b4d9084
"Kouma" Effie cohesive artificial vitreous
TW: “寇瑪”艾飛內聚型人工玻璃體
Taiwan·Risk Class 3·VALEANT MED Sp. z o.o.·Registered May 15, 2012 – May 15, 2027ActiveRegistration details
- Analysis ID
- d9028299ff4ab08770c94aba6b4d9084
- Customs Code
- DHA00602357104
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
- May 15, 2012
- Expiry Date
- May 15, 2027
About this record
Access comprehensive regulatory information for "Kouma" Effie cohesive 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 d9028299ff4ab08770c94aba6b4d9084 and manufactured by VALEANT MED Sp. z o.o.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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