Pure Global

"Helene" retinometer (unsterilized) - Taiwan Registration 0a06d9e8e6666ba3c50689c8bb9ac354

Access comprehensive regulatory information for "Helene" retinometer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0a06d9e8e6666ba3c50689c8bb9ac354 and manufactured by HEINE OPTOTECHNIK GMBH & CO. KG. The authorized representative in Taiwan is CHIU HO MEDICAL SYSTEM 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
0a06d9e8e6666ba3c50689c8bb9ac354
Registration Details
Taiwan FDA Registration: 0a06d9e8e6666ba3c50689c8bb9ac354
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Helene" retinometer (unsterilized)
TW: โ€œๆตท็ณโ€่ฆ–็ถฒ่†œ่จˆ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

0a06d9e8e6666ba3c50689c8bb9ac354

DHA09401405906

Company Information

Product Details

Limited to the first level recognition range of medical equipment management method retinal endoscopy (M.1780).

M Ophthalmology

M.1780 Retinal Lens

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Apr 16, 2014

Apr 16, 2019

Jun 07, 2022

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ