Pure Global

“Riester” Indirect Ophthalmoscope - Taiwan Registration 4ed7077637f1a6fc97abee8959141133

Access comprehensive regulatory information for “Riester” Indirect Ophthalmoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4ed7077637f1a6fc97abee8959141133 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
4ed7077637f1a6fc97abee8959141133
Registration Details
Taiwan FDA Registration: 4ed7077637f1a6fc97abee8959141133
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Riester” Indirect Ophthalmoscope
TW: “雷伊斯特”間接眼底鏡
Risk Class 2
MD

Registration Details

4ed7077637f1a6fc97abee8959141133

Ministry of Health Medical Device Import No. 029769

DHA05602976909

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

Apr 27, 2022

May 25, 2027