Pure Global

"Heidelberg" Streilly retinal imaging diagnostic system - Taiwan Registration 7774b269e0df5b41c67738e89536c596

Access comprehensive regulatory information for "Heidelberg" Streilly retinal imaging diagnostic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7774b269e0df5b41c67738e89536c596 and manufactured by HEIDELBERG ENGINEERING GMBH. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE 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
7774b269e0df5b41c67738e89536c596
Registration Details
Taiwan FDA Registration: 7774b269e0df5b41c67738e89536c596
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Heidelberg" Streilly retinal imaging diagnostic system
TW: โ€œๆตทๅพทๅ กโ€ ๅฒๅด”ๅˆฉ่ฆ–็ถฒ่†œๅฝฑๅƒ่จบๆ–ท็ณป็ตฑ
Risk Class 2

Registration Details

7774b269e0df5b41c67738e89536c596

DHA00602460207

Company Information

Germany

Product Details

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

M Ophthalmology

M.1570 Fundus Mirrors

import

Dates and Status

Jul 08, 2013

Jul 08, 2028