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“CareFusion” V. Mueller Cardiovascular surgical instruments (Non-Sterile) - Taiwan Registration cc9db011531c16e699f0dfb11ab89756

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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cc9db011531c16e699f0dfb11ab89756
Registration Details
Taiwan FDA Registration: cc9db011531c16e699f0dfb11ab89756
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Device Details

“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)
Risk Class 1
MD

Registration Details

cc9db011531c16e699f0dfb11ab89756

Ministry of Health Medical Device Import No. 020144

DHA09402014409

Company Information

Product Details

Limited to the first level identification range of medical equipment management measures for cardiovascular surgical instruments (E.4500).

E Cardiovascular devices

E4500 Cardiovascular Surgical Instrument

Imported from abroad

Dates and Status

Mar 06, 2019

Mar 06, 2024