Taiwan FDA registration 8a2bd9a4b2a4c0b0f54888f2127bf70f
"Rionet" Air Conduction Hearing Aid (Non-sterile)
TW: “瑞愔”氣導式助聽器(未滅菌)
Registration details
- Analysis ID
- 8a2bd9a4b2a4c0b0f54888f2127bf70f
- License Form
- Ministry of Health Medical Device Import No. 021020
- Customs Code
- DHA09402102009
Company information
- Manufacturer
- RION COMPANY, LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- PAO LIEN OPTICAL 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
- Nov 18, 2019
- Expiry Date
- Nov 18, 2024
About this record
Access comprehensive regulatory information for "Rionet" 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 8a2bd9a4b2a4c0b0f54888f2127bf70f and manufactured by RION COMPANY, LTD.. The authorized representative in Taiwan is PAO LIEN OPTICAL CO., LTD..
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