"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.
Device Details
Product Details
Limited to the first level recognition range of medical equipment management method retinal endoscopy (M.1780).
M Ophthalmology
M.1780 Retinal Lens
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Dates and Status
Apr 16, 2014
Apr 16, 2019
Jun 07, 2022
Cancellation Information
Logged out
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