Taiwan FDA registration 9dd82b655cd61060897d8864bd2d9b2f
"plusoptiX" Manual Refractor (Non-Sterile)
TW: "普奧提斯" 手動折射計 (未滅菌)
Taiwan·Risk Class 1·MD·PLUSOPTIX GMBH·Registered Aug 27, 2013 – Aug 27, 2018CancelledRegistration details
- Analysis ID
- 9dd82b655cd61060897d8864bd2d9b2f
- License Form
- Ministry of Health Medical Device Import No. 013335
- Customs Code
- DHA09401333502
Company information
- Manufacturer
- PLUSOPTIX GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- EVERVISION INSTRUMENT CO.
Product details
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1770 Manual Fold Meter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 27, 2013
- Expiry Date
- Aug 27, 2018
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "plusoptiX" Manual Refractor (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9dd82b655cd61060897d8864bd2d9b2f and manufactured by PLUSOPTIX GMBH. The authorized representative in Taiwan is EVERVISION INSTRUMENT CO..
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