Taiwan FDA registration dc999514ac1e9a9f71075933ffcab3b6

"Vibe" Air Conduction hearing aids (Non-Sterile)

TW: "西萬博" 氣導式助聽器 (未滅菌)

Taiwan·Risk Class 1·MD·SIVANTOS PTE LTD·Registered Apr 15, 2020 – Apr 15, 2025Expired

Registration details

Analysis ID: dc999514ac1e9a9f71075933ffcab3b6
License Form: Ministry of Health Medical Device Import No. 021456
Customs Code: DHA09402145607

Company information

Manufacturer: SIVANTOS PTE LTD
Manufacturer Country: Singapore
Authorized Representative: Reap Hearing Group Ltd.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Hearing Aids (G.3300)".
Product Type (Level 1): G ENT device
Product Type (Level 2): G3300 hearing aid
Import Information: Imported from abroad

Dates and status

Registration Date: Apr 15, 2020
Expiry Date: Apr 15, 2025

About this record

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..

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