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"Indomei" Uerkang air-guided hearing aids (unsterilized) - Taiwan Registration ba382eacd229b2c31c4d066d956eb666

Access comprehensive regulatory information for "Indomei" Uerkang 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 ba382eacd229b2c31c4d066d956eb666 and manufactured by UNITRON HEARING GMBH. The authorized representative in Taiwan is Fuling 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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ba382eacd229b2c31c4d066d956eb666
Registration Details
Taiwan FDA Registration: ba382eacd229b2c31c4d066d956eb666
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Device Details

"Indomei" Uerkang air-guided hearing aids (unsterilized)
TW: โ€œ้Ÿณๅคš็พŽโ€ๅ„ช่€ŒๅบทๆฐฃๅฐŽๅผๅŠฉ่ฝๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

ba382eacd229b2c31c4d066d956eb666

DHA04400714900

Company Information

Switzerland

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

Oct 20, 2008

Oct 20, 2018

Jun 17, 2022

Cancellation Information

Logged out

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