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"Intercom" air-directed hearing aids (unsterilized) - Taiwan Registration 56d3062ba2b92cdb50c3e8ddc80a8d9a

Access comprehensive regulatory information for "Intercom" air-directed 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 56d3062ba2b92cdb50c3e8ddc80a8d9a and manufactured by INTERTON A/S. The authorized representative in Taiwan is TRUSTECH 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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56d3062ba2b92cdb50c3e8ddc80a8d9a
Registration Details
Taiwan FDA Registration: 56d3062ba2b92cdb50c3e8ddc80a8d9a
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Device Details

"Intercom" air-directed hearing aids (unsterilized)
TW: โ€œ่‹ฑ็‰น้€šโ€ๆฐฃๅฐŽๅผๅŠฉ่ฝๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

56d3062ba2b92cdb50c3e8ddc80a8d9a

DHA04400686008

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

Jul 02, 2008

Jul 02, 2023

Oct 11, 2024

Cancellation Information

Logged out

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