Taiwan FDA registration cc9db011531c16e699f0dfb11ab89756
“CareFusion” V. Mueller Cardiovascular surgical instruments (Non-Sterile)
TW: “客愛福生”米樂心臟血管外科器械(未滅菌)
Taiwan·Risk Class 1·MD·CareFusion Germany 318 GmbH·Registered Mar 06, 2019 – Mar 06, 2024ExpiredRegistration details
- Analysis ID
- cc9db011531c16e699f0dfb11ab89756
- License Form
- Ministry of Health Medical Device Import No. 020144
- Customs Code
- DHA09402014409
Company information
- Manufacturer
- CareFusion Germany 318 GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- BESPRING INTERNATIONAL MARKETING CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of medical equipment management measures for cardiovascular surgical instruments (E.4500).
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E4500 Cardiovascular Surgical Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 06, 2019
- Expiry Date
- Mar 06, 2024
About this record
Access comprehensive regulatory information for “CareFusion” V. Mueller Cardiovascular surgical instruments (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 cc9db011531c16e699f0dfb11ab89756 and manufactured by CareFusion Germany 318 GmbH. The authorized representative in Taiwan is BESPRING INTERNATIONAL MARKETING CO., LTD..
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