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"Soundton" air-guided hearing aids (unsterilized) - Taiwan Registration f96a5580aaa68906d68ffa9d33a934c1

Access comprehensive regulatory information for "Soundton" air-guided hearing aids (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f96a5580aaa68906d68ffa9d33a934c1 and manufactured by INTERTON A/S. The authorized representative in Taiwan is Xingxuan Technology 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.

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f96a5580aaa68906d68ffa9d33a934c1
Registration Details
Taiwan FDA Registration: f96a5580aaa68906d68ffa9d33a934c1
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Device Details

"Soundton" air-guided hearing aids (unsterilized)
TW: โ€œ้Ÿณๅพ—้€šโ€ๆฐฃๅฐŽๅผๅŠฉ่ฝๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

f96a5580aaa68906d68ffa9d33a934c1

DHA04400868602

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 Science

G.3300 Hearing Aids

import

Dates and Status

Apr 07, 2010

Apr 07, 2020

Jan 23, 2019

Cancellation Information

Logged out

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