Pure Global

“Riester” ri-scope L Ophthalmoscope - Taiwan Registration a4b2cbfa1b6d1976150677c2e094f78b

Access comprehensive regulatory information for “Riester” ri-scope L Ophthalmoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a4b2cbfa1b6d1976150677c2e094f78b and manufactured by Rudolf Riester GmbH. The authorized representative in Taiwan is JUN FENG OPTICAL CO., LTD..

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
a4b2cbfa1b6d1976150677c2e094f78b
Registration Details
Taiwan FDA Registration: a4b2cbfa1b6d1976150677c2e094f78b
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Riester” ri-scope L Ophthalmoscope
TW: “雷伊斯特”直接眼底鏡
Risk Class 2
MD

Registration Details

a4b2cbfa1b6d1976150677c2e094f78b

Ministry of Health Medical Device Import No. 029115

DHA05602911501

Company Information

Germany

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

Nov 21, 2016

Nov 21, 2026