Taiwan FDA registration 30ced7a35f83fae5f9572848d4186e99
"Ruineng IOL guide" (sterilization)
TW: “銳能”人工水晶體導引器（滅菌）
Taiwan·Risk Class 1·RAYNER INTRAOCULAR LENSES LTD.·Registered Mar 13, 2007 – Mar 13, 2022CancelledRegistration details
- Analysis ID
- 30ced7a35f83fae5f9572848d4186e99
- Customs Code
- DHA04400566709
Company information
- Manufacturer
- RAYNER INTRAOCULAR LENSES LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- UNITED MEDICAL INC.
Product details
- Intended Use
- Limited to the first level identification range of "Intraocular Lens Guide (M.4300)" under the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4300 Artificial crystal body inducer
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Mar 13, 2007
- Expiry Date
- Mar 13, 2022
- Cancellation Date
- Sep 27, 2021
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Ruineng IOL guide" (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 30ced7a35f83fae5f9572848d4186e99 and manufactured by RAYNER INTRAOCULAR LENSES LTD.. The authorized representative in Taiwan is UNITED MEDICAL INC..
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