Taiwan FDA registration 3506177c232736fbd71d26d6888b3107
"Odi" audiometer (unsterilized)
TW: "歐迪"聽力檢查計(未滅菌)
Taiwan·Risk Class 1·AUDITDATA A/S·Registered Feb 08, 2018 – Feb 08, 2023ExpiredRegistration details
- Analysis ID
- 3506177c232736fbd71d26d6888b3107
- Customs Code
- DHA09401879901
Company information
- Manufacturer
- AUDITDATA A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- MELODY MEDICAL INSTRUMENTS CORPORATION
Product details
- Intended Use
- Limited to the first-level recognition range of the Measures for the Administration of Medical Devices "Audiogrammeter (G.1050)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.1050 Audiometer
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Feb 08, 2018
- Expiry Date
- Feb 08, 2023
About this record
Access comprehensive regulatory information for "Odi" audiometer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3506177c232736fbd71d26d6888b3107 and manufactured by AUDITDATA A/S. The authorized representative in Taiwan is MELODY MEDICAL INSTRUMENTS CORPORATION.
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