Taiwan FDA registration 4f3db0c4d9442f0fa3d704903aa29b39
"Siemens" full range of gas-guided hearing aids (unsterilized)
TW: “西門子”全系列氣導式助聽器 (未滅菌)
Taiwan·Risk Class 1·SIEMENS MEDICAL INSTRUMENTS PTE LTD·Registered Jan 18, 2008 – Jan 18, 2018CancelledRegistration details
- Analysis ID
- 4f3db0c4d9442f0fa3d704903aa29b39
- Customs Code
- DHA04400647008
Company information
- Manufacturer
- SIEMENS MEDICAL INSTRUMENTS PTE LTD
- Manufacturer Country
- Singapore
- Authorized Representative
- EARLINK TECHNOLOGY 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
- Jan 18, 2008
- Expiry Date
- Jan 18, 2018
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Siemens" full range of gas-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 4f3db0c4d9442f0fa3d704903aa29b39 and manufactured by SIEMENS MEDICAL INSTRUMENTS PTE LTD. The authorized representative in Taiwan is EARLINK TECHNOLOGY CO., LTD..
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