Taiwan FDA registration bd6ea65d81c555abd3ec33a47472c2e9
“CenterVue” DRSplus
TW: “善待優” 眼底鏡
Taiwan·Risk Class 2·MD·Centervue S.p.A.·Registered Apr 14, 2021 – Apr 14, 2026ExpiredRegistration details
- Analysis ID
- bd6ea65d81c555abd3ec33a47472c2e9
- License Form
- Ministry of Health Medical Device Import No. 034499
- Customs Code
- DHA05603449900
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
- Apr 14, 2021
- Expiry Date
- Apr 14, 2026
About this record
Access comprehensive regulatory information for “CenterVue” DRSplus in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bd6ea65d81c555abd3ec33a47472c2e9 and manufactured by Centervue S.p.A.. The authorized representative in Taiwan is BioLaden Consultant Corp..
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