Taiwan FDA registration fa769314222b22f1791661320d75f4f3
"Phastema" ophthalmic test lens set (unsterilized)
TW: "飛司特馬"眼科試驗鏡片組(未滅菌)
Taiwan·Risk Class 1·FRASTEMA S.R.L.·Registered Aug 03, 2012 – Aug 03, 2022CancelledRegistration details
- Analysis ID
- fa769314222b22f1791661320d75f4f3
- Customs Code
- DHA04401203107
Company information
- Manufacturer
- FRASTEMA S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- JUN FENG OPTICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the ophthalmic test lens group (M.1405) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1405 眼科試驗鏡片組
- Import Information
- import
Dates and status
- Registration Date
- Aug 03, 2012
- Expiry Date
- Aug 03, 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 "Phastema" ophthalmic test lens set (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fa769314222b22f1791661320d75f4f3 and manufactured by FRASTEMA S.R.L.. The authorized representative in Taiwan is JUN FENG OPTICAL CO., LTD..
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