Taiwan FDA registration 22b6157eebcb5f9670811aa329ad5ad7
"Freiyfang" audiogram (unsterilized)
TW: “佛賴伊芳” 聽力檢查計 (未滅菌)
Taiwan·Risk Class 1·FRYE ELECTRONICS INC.·Registered Mar 11, 2013 – Mar 11, 2018CancelledRegistration details
- Analysis ID
- 22b6157eebcb5f9670811aa329ad5ad7
- Customs Code
- DHA04401278506
Company information
- Manufacturer
- FRYE ELECTRONICS INC.
- Manufacturer Country
- United States
- Authorized Representative
- GREAT SOUND 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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Mar 11, 2013
- Expiry Date
- Mar 11, 2018
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Freiyfang" audiogram (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 22b6157eebcb5f9670811aa329ad5ad7 and manufactured by FRYE ELECTRONICS INC.. The authorized representative in Taiwan is GREAT SOUND 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