Pure Global

“CenterVue” DRSplus - Taiwan Registration bd6ea65d81c555abd3ec33a47472c2e9

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free Database
Powered by Pure Global AI
89,000+ Devices
bd6ea65d81c555abd3ec33a47472c2e9
Registration Details
Taiwan FDA Registration: bd6ea65d81c555abd3ec33a47472c2e9
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“CenterVue” DRSplus
TW: “善待優” 眼底鏡
Risk Class 2
MD

Registration Details

bd6ea65d81c555abd3ec33a47472c2e9

Ministry of Health Medical Device Import No. 034499

DHA05603449900

Company Information

Italy

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmic devices

M1570 fundus mirror

Imported from abroad

Dates and Status

Apr 14, 2021

Apr 14, 2026