Taiwan FDA registration 922b130837062578846e920dcc892d3a
"Signia" Hearing Aid (Non-Sterile)
TW: "西嘉" 助聽器 (未滅菌)
Taiwan·Risk Class 1·MD·SIVANTOS PTE LTD·Registered Jun 04, 2019 – Jun 04, 2024ExpiredRegistration details
- Analysis ID
- 922b130837062578846e920dcc892d3a
- License Form
- Ministry of Health Medical Device Import No. 020521
- Customs Code
- DHA09402052100
Company information
- Manufacturer
- SIVANTOS PTE LTD
- Manufacturer Country
- Singapore
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
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 04, 2019
- Expiry Date
- Jun 04, 2024
About this record
Access comprehensive regulatory information for "Signia" 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 922b130837062578846e920dcc892d3a and manufactured by SIVANTOS PTE LTD. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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