Taiwan FDA registration 40380d45080e8d61c7a568daba3b9ce7
"Siemens" air-guided hearing aids (unsterilized)
TW: "西門子"氣導助聽器 (未滅菌)
Taiwan·Risk Class 1·SIEMENS MEDICAL INSTRUMENTS PTE LTD·Registered Apr 26, 2006 – Apr 26, 2021CancelledRegistration details
- Analysis ID
- 40380d45080e8d61c7a568daba3b9ce7
- Customs Code
- DHA04400423208
Company information
- Manufacturer
- SIEMENS MEDICAL INSTRUMENTS PTE LTD
- Manufacturer Country
- Singapore
- Authorized Representative
- TAIWAN VAPOR CORPORATION
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
- Apr 26, 2006
- Expiry Date
- Apr 26, 2021
- Cancellation Date
- Sep 21, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Siemens" 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 40380d45080e8d61c7a568daba3b9ce7 and manufactured by SIEMENS MEDICAL INSTRUMENTS PTE LTD. The authorized representative in Taiwan is TAIWAN VAPOR CORPORATION.
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