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"Interton" Hearing Aids (Non-Sterile) - Taiwan Registration d1e757592a5aea7fe83358ecb303b537

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 d1e757592a5aea7fe83358ecb303b537 and manufactured by INTERTON A/S. The authorized representative in Taiwan is TAIWAN VAPOR CORPORATION.

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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d1e757592a5aea7fe83358ecb303b537
Registration Details
Taiwan FDA Registration: d1e757592a5aea7fe83358ecb303b537
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Device Details

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

Registration Details

d1e757592a5aea7fe83358ecb303b537

Ministry of Health Medical Device Import No. 015993

DHA09401599308

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 18, 2015

Dec 18, 2025

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