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"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.

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a86aa3981d54e1a2ca8775dc344480fe
Registration Details
Taiwan FDA Registration: a86aa3981d54e1a2ca8775dc344480fe
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Device Details

"Interton" Hearing Aids (Non-Sterile)
TW: "้Ÿณๅพท้€š" ๅŠฉ่ฝๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

a86aa3981d54e1a2ca8775dc344480fe

Ministry of Health Medical Device Import No. 017309

DHA09401730905

Company Information

Denmark

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

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