Taiwan FDA registration 118398d17d7bdd0d914d5c1bf730409d
"Mueryan" Errui intraocular lens
TW: “目爾艷”愛芮人工水晶體
Taiwan·Risk Class 3·MORCHER GMBH·Registered Dec 14, 2010 – Dec 14, 2025CancelledRegistration details
- Analysis ID
- 118398d17d7bdd0d914d5c1bf730409d
- Customs Code
- DHA00602179108
Company information
- Manufacturer
- MORCHER GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- HEALTH CARE MEDICAL INC.
Product details
- Intended Use
- Used to replace normal lentles or patients requiring iridescent reconstruction in the following described cases, such as: 1. congenital or acquired anisis, 2. traumatic aniridia, 3. partial absence of iris, 4. albinism (congenital pigment deficiency). (This product is not required for cataract or alens patients).
- Product Type (Level 1)
- M Ophthalmology
- Import Information
- import
Dates and status
- Registration Date
- Dec 14, 2010
- Expiry Date
- Dec 14, 2025
- Cancellation Date
- Sep 15, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Mueryan" Errui 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 118398d17d7bdd0d914d5c1bf730409d and manufactured by MORCHER GMBH. The authorized representative in Taiwan is HEALTH CARE MEDICAL INC..
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