Taiwan FDA registration ca529fd19052dcba677a01d9e2e1f30f
"National" Reston hearing aids (unsterilized)
TW: “全國”力斯頓助聽器（未滅菌）
Taiwan·Risk Class 1·SIEMENS MEDICAL INSTRUMENTS PTE LTD·Registered Oct 27, 2010 – Oct 27, 2020CancelledRegistration details
- Analysis ID
- ca529fd19052dcba677a01d9e2e1f30f
- Customs Code
- DHA04400929709
Company information
- Manufacturer
- SIEMENS MEDICAL INSTRUMENTS PTE LTD
- 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 Science
- Product Type (Level 2)
- G.3300 Hearing Aids
- Import Information
- import
Dates and status
- Registration Date
- Oct 27, 2010
- Expiry Date
- Oct 27, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "National" Reston 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 ca529fd19052dcba677a01d9e2e1f30f and manufactured by SIEMENS MEDICAL INSTRUMENTS PTE LTD. The authorized representative in Taiwan is ALLDAY HEARING AID CO., LTD..
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