Taiwan FDA registration db5dcfaae503e2317331580e51985ee6
“CenterVue” Digital Retina Scanning Ophthalmoscope
TW: “先得優”數位視網膜掃描眼底鏡
Taiwan·Risk Class 2·MD·Centervue S.p.A.·Registered Nov 06, 2017 – Nov 06, 2027ActiveRegistration details
- Analysis ID
- db5dcfaae503e2317331580e51985ee6
- License Form
- Ministry of Health Medical Device Import No. 030410
- Customs Code
- DHA05603041003
Company information
- Manufacturer
- Centervue S.p.A.
- Manufacturer Country
- Italy
- Authorized Representative
- BioLaden Consultant Corp.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1570 fundus mirror
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 06, 2017
- Expiry Date
- Nov 06, 2027
About this record
Access comprehensive regulatory information for “CenterVue” Digital Retina Scanning Ophthalmoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number db5dcfaae503e2317331580e51985ee6 and manufactured by Centervue S.p.A.. The authorized representative in Taiwan is BioLaden Consultant Corp..
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