Taiwan FDA registration fdb08f018b118bf04440dac80d9413f8
"Siemens" hearing aid analysis system
TW: “西門子”優能儀助聽器分析系統
Taiwan·Risk Class 2·SIEMENS AUDIOLOGISCHE TECHNIK GMBH; INTERACOUSTICS A/S·Registered Mar 27, 2013 – Mar 27, 2018CancelledRegistration details
- Analysis ID
- fdb08f018b118bf04440dac80d9413f8
- Customs Code
- DHA00602482402
Company information
- Manufacturer Country
- Germany;;Denmark
- Authorized Representative
- SIEMENS LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.3310 Hearing Aid Correctors and Analysis Systems
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Mar 27, 2013
- Expiry Date
- Mar 27, 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 "Siemens" hearing aid analysis system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fdb08f018b118bf04440dac80d9413f8 and manufactured by SIEMENS AUDIOLOGISCHE TECHNIK GMBH; INTERACOUSTICS A/S. The authorized representative in Taiwan is SIEMENS LIMITED.
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