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"INTERTON" Hearing Aid (Non-Sterile) - Taiwan Registration 3d19e6fe747bb32e99704642881fd8ff

Access comprehensive regulatory information for "INTERTON" Hearing Aid (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 3d19e6fe747bb32e99704642881fd8ff and manufactured by INTERTON (GN RESOUND AS). The authorized representative in Taiwan is GREAT SOUND 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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3d19e6fe747bb32e99704642881fd8ff
Registration Details
Taiwan FDA Registration: 3d19e6fe747bb32e99704642881fd8ff
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Device Details

"INTERTON" Hearing Aid (Non-Sterile)
TW: "ๅพท้Ÿณ"ๅŠฉ่ฝๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

3d19e6fe747bb32e99704642881fd8ff

Ministry of Health Medical Device Import No. 016228

DHA09401622800

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

Mar 04, 2016

Mar 04, 2021