Taiwan FDA registration 33aa5c36e57fff8c67690a8547ffcff7
"Fulai" Fonnix Audioexaminer (unsterilized)
TW: “富來”方尼克斯聽力檢查儀（未滅菌）
Taiwan·Risk Class 1·FRYE ELECTRONICS, INC.·Registered Mar 23, 2010 – Mar 23, 2020CancelledRegistration details
- Analysis ID
- 33aa5c36e57fff8c67690a8547ffcff7
- Customs Code
- DHA04400863702
Company information
- Manufacturer
- FRYE ELECTRONICS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- KING PAX TECHNOLOGY CO., LTD.
Product details
- Intended Use
- Limited to the first-level recognition range of the Measures for the Administration of Medical Devices "Audiogrammeter (G.1050)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.1050 Audiometer
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Mar 23, 2010
- Expiry Date
- Mar 23, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Fulai" Fonnix Audioexaminer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 33aa5c36e57fff8c67690a8547ffcff7 and manufactured by FRYE ELECTRONICS, INC.. The authorized representative in Taiwan is KING PAX TECHNOLOGY 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