7 results
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25ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
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MINIMED QUICK-SET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·July 7, 2025
OT VERIO TEST STRIPS
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 14, 2013
IACCU-CHEK SPIRIT
FDA Adverse Event
Malfunction
·DISETRONIC MEDICAL SYSTEMS·Product code LZG·February 20, 2008
LUMENIS PULSE 30H
FDA Adverse Event
Malfunction
·LUMENIS LTD.·Product code GEX·November 12, 2020
LUMENIS PULSE 30H
FDA Adverse Event
Malfunction
·LUMENIS LTD.·Product code GEX·February 17, 2022
LUMENIS PULSE 30H
FDA Adverse Event
Malfunction
·LUMENIS LTD.·Product code GEX·March 30, 2022
LUMENIS PULSE 30H
FDA Adverse Event
Malfunction
·LUMENIS LTD.·Product code GEX·January 13, 2022