Taiwan FDA registration 18807346ef114171317eb47d3d4bcbbf
"Puotis" ophthalmic refractive machine (unsterilized)
TW: "普奧提斯" 眼科驗光機 (未滅菌)
Taiwan·Risk Class 1·PLUSOPTIX GMBH·Registered Sep 30, 2016 – Sep 30, 2021CancelledRegistration details
- Analysis ID
- 18807346ef114171317eb47d3d4bcbbf
- Customs Code
- DHA09401703800
Company information
- Manufacturer
- PLUSOPTIX GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- EVERVISION INSTRUMENT CO.
Product details
- Intended Use
- Limited to the first level recognition range of ophthalmic optometry machine (M.1760) of the management measures for medical equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1760 Automatic Ophthalmic Optical Machine
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Sep 30, 2016
- Expiry Date
- Sep 30, 2021
- Cancellation Date
- Sep 08, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Puotis" ophthalmic refractive machine (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 18807346ef114171317eb47d3d4bcbbf and manufactured by PLUSOPTIX GMBH. The authorized representative in Taiwan is EVERVISION INSTRUMENT CO..
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