"Interton" Hearing Aids (Non-Sterile) - Taiwan Registration a86aa3981d54e1a2ca8775dc344480fe
Access comprehensive regulatory information for "Interton" Hearing Aids (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a86aa3981d54e1a2ca8775dc344480fe and manufactured by INTERTON A/S. The authorized representative in Taiwan is MERRY FULING CO., LTD., TAIWAN BRANCH (SAMOA).
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including INTERTON A/S, and 2 recent registrations in the same category. 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
Registration Details
a86aa3981d54e1a2ca8775dc344480fe
Ministry of Health Medical Device Import No. 017309
DHA09401730905
Product Details
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Hearing Aids (G.3300)".
G ENT device
G3300 hearing aid
Imported from abroad
Dates and Status
Dec 20, 2016
Dec 20, 2021

