28 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PHILIPS XRG 90 X-RAY GENERATOR SYSTEM
FDA 510(k)
FDA Class 1
·Radiology
CAPSTONE SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ACUNAV 90/10 DIAGNOSTIC ULTRASOUND CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·May 25, 2012
HOLDING FORCEPS 170MM
FDA Adverse Event
Malfunction
·SYNTHES SALZBURG·Product code HTD·October 10, 2016
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·October 30, 2012
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 6, 2012
INTERSTIM II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code EZW·August 7, 2012
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·August 17, 2012
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·December 11, 2013
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·August 20, 2014
ASR UNI FEMORAL IMPL SIZE 53
FDA Adverse Event
Injury
·Product code KWA·December 17, 2010
HAKIM VENTRICULAR & PERITONEAL CATHETERS WITH BACTISEAL
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC·Product code JXG·January 29, 2013
OT VERIO TEST STRIPS
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 15, 2014
PS TIBIAL INSERTS SZ 4, 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·April 14, 2023
CC FEMORAL SZ 3
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·October 10, 2024
CEMENTED FINNED TIB. TRA SZ 3F/3T
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·December 19, 2024
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·November 26, 2014
OPTETRAK KNEE SYSTEM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·July 23, 2024
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·April 8, 2013