Taiwan FDA registration 7b44da6dbdf3f8f36a2210edb3f9228e

"Sonova" Air Conduction Hearing Aid (Non-Sterile)

TW: "索諾瓦" 氣導式助聽器 (未滅菌)

Taiwan·Risk Class 1·MD·Sonova AG·Registered Jun 01, 2020 – Jun 01, 2025Expired

Registration details

Analysis ID: 7b44da6dbdf3f8f36a2210edb3f9228e
License Form: Ministry of Health Medical Device Import No. 021602
Customs Code: DHA09402160205

Company information

Manufacturer: Sonova AG
Manufacturer Country: Switzerland
Authorized Representative: JEN SOUND ENTERPRISE CO., 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: Jun 01, 2020
Expiry Date: Jun 01, 2025

About this record

Access comprehensive regulatory information for "Sonova" Air Conduction 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 7b44da6dbdf3f8f36a2210edb3f9228e and manufactured by Sonova AG. The authorized representative in Taiwan is JEN SOUND ENTERPRISE CO., LTD..

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