Taiwan FDA registration b0651df20feccda37e505b3a81aca8db
"Virtue Heart" intraocular lens guide (sterilization)
TW: “美德心”人工水晶體導引器（滅菌）
Taiwan·Risk Class 1·ROBUTEC AG;; MEDICEL AG·Registered Sep 04, 2013 – Sep 04, 2028ActiveRegistration details
- Analysis ID
- b0651df20feccda37e505b3a81aca8db
- Customs Code
- DHA09401337501
Company information
- Manufacturer
- ROBUTEC AG;; MEDICEL AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- UNITED MEDICAL INC.
Product details
- Intended Use
- Limited to the first level identification range of "intraocular lens guide (M.4300)" of the Classification and Grading Management Measures for Medical Equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4300 Artificial crystal body inducer
- Import Information
- QMS/QSD;; 輸入;; 委託製造
Dates and status
- Registration Date
- Sep 04, 2013
- Expiry Date
- Sep 04, 2028
About this record
Access comprehensive regulatory information for "Virtue Heart" intraocular lens 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 b0651df20feccda37e505b3a81aca8db and manufactured by ROBUTEC AG;; MEDICEL AG. The authorized representative in Taiwan is UNITED MEDICAL INC..
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