Taiwan FDA registration a65e3f4412f7af633da743c74ea3f7af
“Aesculap” General purpose medical instruments cleaner (Non-sterile)
TW: “雅氏” 一般醫療器械用清潔劑(未滅菌)
Taiwan·Risk Class 1·MD·AESCULAP AG·Registered Sep 23, 2020 – Sep 23, 2025ExpiredRegistration details
- Analysis ID
- a65e3f4412f7af633da743c74ea3f7af
- License Form
- Ministry of Health Medical Device Import No. 021979
- Customs Code
- DHA09402197900
Company information
- Manufacturer
- AESCULAP AG
- Manufacturer Country
- Germany
- Authorized Representative
- B. BRAUN TAIWAN CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Disinfectants for General Medical Devices (J.6890)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6890 Disinfectants for general medical devices
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 23, 2020
- Expiry Date
- Sep 23, 2025
About this record
Access comprehensive regulatory information for “Aesculap” General purpose medical instruments cleaner (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a65e3f4412f7af633da743c74ea3f7af and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..
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