Taiwan FDA registration 864afb9be38298b800522d8875ba136b
"Automejis" Madison Hearing Examiner (Unsterilized)
TW: "歐托邁吉司" 麥迪生聽力檢查儀 (未滅菌)
Taiwan·Risk Class 1·NATUS MEDICAL DENMARK APS·Registered Dec 06, 2012 – Dec 06, 2022CancelledRegistration details
- Analysis ID
- 864afb9be38298b800522d8875ba136b
- Customs Code
- DHA04401244801
Company information
- Manufacturer
- NATUS MEDICAL DENMARK APS
- Manufacturer Country
- Denmark
- Authorized Representative
- FORMOSA MEDICAL INSTRUMENTS CO., LTD.
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
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Dec 06, 2012
- Expiry Date
- Dec 06, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Automejis" Madison Hearing Examiner (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 864afb9be38298b800522d8875ba136b and manufactured by NATUS MEDICAL DENMARK APS. The authorized representative in Taiwan is FORMOSA MEDICAL INSTRUMENTS CO., LTD..
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