Taiwan FDA registration 068a05d6e720e45a704144caf6e618fa
"Argosy" Hearing Aid (Non-Sterile)
TW: "瑞士雅歌" 助聽器 (未滅菌)
Taiwan·Risk Class 1·MD·Sonova Operation Center Vietnam Co., Ltd·Registered Mar 30, 2020 – Mar 30, 2025ExpiredRegistration details
- Analysis ID
- 068a05d6e720e45a704144caf6e618fa
- License Form
- Ministry of Health Medical Device Import No. 021412
- Customs Code
- DHA09402141200
Company information
- Manufacturer
- Sonova Operation Center Vietnam Co., Ltd
- Manufacturer Country
- Viet Nam
- Authorized Representative
- SONOVA TAIWAN PTE 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
- Mar 30, 2020
- Expiry Date
- Mar 30, 2025
About this record
Access comprehensive regulatory information for "Argosy" 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 068a05d6e720e45a704144caf6e618fa and manufactured by Sonova Operation Center Vietnam Co., Ltd. The authorized representative in Taiwan is SONOVA TAIWAN PTE 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.
Free DatabasePowered by Pure Global AI89,000+ Devices