Taiwan FDA registration f5bd37b29475bd96f9f95abceaac8675
"Ruineng " Ruiweishi artificial vitreous
TW: “銳能”瑞威視人工玻璃體
Taiwan·Risk Class 3·RAYNER INTRAOCULAR LENSES LTD.·Registered Dec 19, 2007 – Dec 19, 2022CancelledRegistration details
- Analysis ID
- f5bd37b29475bd96f9f95abceaac8675
- Customs Code
- DHA00601850602
Company information
- Manufacturer
- RAYNER INTRAOCULAR LENSES LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- UNITED MEDICAL INC.
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
- Dec 19, 2007
- Expiry Date
- Dec 19, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Ruineng " Ruiweishi 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 f5bd37b29475bd96f9f95abceaac8675 and manufactured by RAYNER INTRAOCULAR LENSES LTD.. The authorized representative in Taiwan is UNITED MEDICAL INC..
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