85 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
DJO SURGICAL REVISION FEMORAL HIP SYSTEM, MODEL 428-14/24-140/200; 428-00-050/110;
FDA 510(k)
FDA Class 3
·Orthopedic
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04047872673174·LEVAMED STABILI-TRI ANK BLU R I
PROFILE-ER
FDA 510(k)
FDA Class 2
·Clinical Toxicology
ADVIA 120 HEMATOLOGY SYSTEM, CEREBROSPINAL FLUID METHOD
FDA 510(k)
FDA Class 2
·Hematology
PERFUSOR®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FRN·April 10, 2025
NEOCIF INSERTION INSTRUMENT
FDA Adverse Event
Malfunction
·BIOMET SPAIN, S.L.·Product code MQP·November 6, 2018
PERFUSOR®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FRN·May 5, 2025
PERFUSOR®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FRN·May 13, 2026
PERFUSOR®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FRN·April 14, 2026
PERFUSOR®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FRN·May 18, 2026
PERFUSOR®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FRN·May 19, 2025
PERFUSOR®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FRN·May 19, 2025
PERFUSOR®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FRN·April 8, 2025
NEOCIF INSERTION INSTRUMENT
FDA Adverse Event
Malfunction
·BIOMET SPAIN, S.L.·Product code MQP·July 20, 2017
PERFUSOR®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FRN·March 30, 2026
PERFUSOR®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FRN·March 31, 2026
NC TREK CORONARY DILATATION CATHETER
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code LOX·May 3, 2013
840 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN·Product code CBK·August 19, 2014
GOBED II
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·May 3, 2011
PERFUSOR®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FRN·April 6, 2026