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"ALL DAY" Hearing Aid (Non-Sterile) - Taiwan Registration 20b814229a804064028b8ebd70275d7a

Access comprehensive regulatory information for "ALL DAY" 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 20b814229a804064028b8ebd70275d7a and manufactured by SIVANTOS GMBH. The authorized representative in Taiwan is ALLDAY HEARING AID 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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20b814229a804064028b8ebd70275d7a
Registration Details
Taiwan FDA Registration: 20b814229a804064028b8ebd70275d7a
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Device Details

"ALL DAY" Hearing Aid (Non-Sterile)
TW: "ๅ…จๅœ‹" ๅŠฉ่ฝๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

20b814229a804064028b8ebd70275d7a

Ministry of Health Medical Device Import No. 018544

DHA09401854407

Company Information

Singapore

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

Nov 23, 2017

Nov 23, 2022