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"Vibe" Air Conduction hearing aids (Non-Sterile) - Taiwan Registration dc999514ac1e9a9f71075933ffcab3b6

Access comprehensive regulatory information for "Vibe" Air Conduction 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 dc999514ac1e9a9f71075933ffcab3b6 and manufactured by SIVANTOS PTE LTD. The authorized representative in Taiwan is Reap Hearing Group 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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dc999514ac1e9a9f71075933ffcab3b6
Registration Details
Taiwan FDA Registration: dc999514ac1e9a9f71075933ffcab3b6
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Device Details

"Vibe" Air Conduction hearing aids (Non-Sterile)
TW: "่ฅฟ่ฌๅš" ๆฐฃๅฐŽๅผๅŠฉ่ฝๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

dc999514ac1e9a9f71075933ffcab3b6

Ministry of Health Medical Device Import No. 021456

DHA09402145607

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

Apr 15, 2020

Apr 15, 2025