Taiwan FDA registration d5f10eb7d54f2edb9b2304ff56de7c13
"Puotis" keratoscope (unsterilized)
TW: “普奧提斯”角膜鏡(未滅菌)
Taiwan·Risk Class 1·PLUSOPTIX GMBH·Registered Sep 26, 2012 – Sep 26, 2017CancelledRegistration details
- Analysis ID
- d5f10eb7d54f2edb9b2304ff56de7c13
- Customs Code
- DHA04401220501
Company information
- Manufacturer
- PLUSOPTIX GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- EVERVISION INSTRUMENT CO.
Product details
- Intended Use
- Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1350 Coratoscope
- Import Information
- import
Dates and status
- Registration Date
- Sep 26, 2012
- Expiry Date
- Sep 26, 2017
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Puotis" keratoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d5f10eb7d54f2edb9b2304ff56de7c13 and manufactured by PLUSOPTIX GMBH. The authorized representative in Taiwan is EVERVISION INSTRUMENT CO..
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