Taiwan FDA registration 9a85cf2d2e44c11472bc038530e805da
"Pulton" air-guided hearing aids (unsterilized)
TW: “普耳通”氣導助聽器 (未滅菌)
Taiwan·Risk Class 1·PURETONE LTD.·Registered Feb 17, 2009 – Feb 17, 2014CancelledRegistration details
- Analysis ID
- 9a85cf2d2e44c11472bc038530e805da
- Customs Code
- DHA04400749302
Company information
- Manufacturer
- PURETONE LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- JEN SOUND ENTERPRISE 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 Science
- Product Type (Level 2)
- G.3300 Hearing Aids
- Import Information
- import
Dates and status
- Registration Date
- Feb 17, 2009
- Expiry Date
- Feb 17, 2014
- Cancellation Date
- Jan 09, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Pulton" air-guided hearing aids (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9a85cf2d2e44c11472bc038530e805da and manufactured by PURETONE LTD.. The authorized representative in Taiwan is JEN SOUND ENTERPRISE CO., LTD..
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