Taiwan FDA registration 20b814229a804064028b8ebd70275d7a
"ALL DAY" Hearing Aid (Non-Sterile)
TW: "全國" 助聽器 (未滅菌)
Taiwan·Risk Class 1·MD·SIVANTOS GMBH·Registered Nov 23, 2017 – Nov 23, 2022ExpiredRegistration details
- Analysis ID
- 20b814229a804064028b8ebd70275d7a
- License Form
- Ministry of Health Medical Device Import No. 018544
- Customs Code
- DHA09401854407
Company information
- Manufacturer
- SIVANTOS GMBH
- Manufacturer Country
- Singapore
- Authorized Representative
- ALLDAY HEARING AID 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 23, 2017
- Expiry Date
- Nov 23, 2022
About this record
Access comprehensive regulatory information for "ALL DAY" 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 20b814229a804064028b8ebd70275d7a and manufactured by SIVANTOS GMBH. The authorized representative in Taiwan is ALLDAY HEARING AID CO., 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