124 results · 22ms · Sources: EU EUDAMED, US FDA

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AccuLIF TL and PL Cage

FDA 510(k)
FDA Class 2 ·Orthopedic

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526550216·GENUMEDI PT KNEE SUP SILVER R EW VI

T PLATE

FDA UDI
Biomet Orthopedics, LLC·00887868004544·

ACCUDXA2

FDA 510(k)
FDA Class 2 ·Radiology

PINPOINT STEREOTACTIC HEAD AND NECK LOCALIZER

FDA 510(k)
FDA Class 2 ·Radiology

ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·December 16, 2020

ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·October 27, 2020

ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·October 22, 2020

8100 ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·March 21, 2022

UNKNOWN DEPUY LPS FEMORAL COMPONENT

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·October 6, 2014

RESERVOIR 3ML

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·June 3, 2013

CARDIOPULMONARY DEVICE

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DTQ·June 3, 2011

ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·October 23, 2020

ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·November 6, 2020

ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·November 6, 2020

ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·December 5, 2020

ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·December 10, 2020

ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·October 30, 2020

ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·November 2, 2020

ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·November 13, 2020