Taiwan FDA registration 2e4d5c28cf8bb3adcae714797c806de4
"We hear" AC hearing aids (Non-Sterile)
TW: "維膜" 氣導助聽器 (未滅菌)
Taiwan·Risk Class 1·MD·SIVANTOS PTE LTD·Registered Aug 23, 2017 – Aug 23, 2022ExpiredRegistration details
- Analysis ID
- 2e4d5c28cf8bb3adcae714797c806de4
- License Form
- Ministry of Health Medical Device Import No. 018233
- Customs Code
- DHA09401823303
Company information
- Manufacturer
- SIVANTOS PTE LTD
- Manufacturer Country
- Singapore
- Authorized Representative
- TAIWAN VAPOR 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
- Aug 23, 2017
- Expiry Date
- Aug 23, 2022
About this record
Access comprehensive regulatory information for "We hear" AC 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 2e4d5c28cf8bb3adcae714797c806de4 and manufactured by SIVANTOS PTE LTD. The authorized representative in Taiwan is TAIWAN VAPOR CORPORATION.
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