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"Interton" Hearing Aids (Non-Sterile) - Taiwan Registration b91f3aa40f16f626b408f0efc9d0b609

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 b91f3aa40f16f626b408f0efc9d0b609 and manufactured by INTERTON A/S. The authorized representative in Taiwan is Hongyun Medical Equipment Co., Ltd.

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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b91f3aa40f16f626b408f0efc9d0b609
Registration Details
Taiwan FDA Registration: b91f3aa40f16f626b408f0efc9d0b609
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Device Details

"Interton" Hearing Aids (Non-Sterile)
TW: "้Ÿณ็‰น่€ณ" ๅŠฉ่ฝๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

b91f3aa40f16f626b408f0efc9d0b609

Ministry of Health Medical Device Import No. 017037

DHA09401703701

Company Information

Denmark

Product Details

G ENT device

G3300 hearing aid

Imported from abroad

Dates and Status

Sep 30, 2016

Sep 30, 2021

Jan 18, 2019

Cancellation Information

Logged out

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