80 results
·
19ms
·
Sources: EU EUDAMED, US FDA
PULSE GENERATORS MODELS 657 & 677
FDA 510(k)
FDA Class 3
·Cardiovascular
ADVIA Centaur® Systems aHBs2 MCM
FDA UDI
Siemens Healthcare Diagnostics Inc.·00630414555300·aHBs2 Master Curve Material
0800,APS0,08,N,LT,RDL,NO VOL,RW,TB
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828153003·0800,APS0,08,N,LT,RDL,NO VOL,RW,TB
ACUMED
FDA UDI
Acumed LLC·10806378041778·2.8mm Quick Release Drill
Acumed
FDA UDI
Provision·B504OM8003870·
Acumed
FDA UDI
Provision·00810041060877·
Reprocessed 2.8mm Quick Release Drill Bit
FDA UDI
SURETEK MEDICAL·B3908003871·
NA
FDA UDI
STERILMED, INC.·10888551004770·DRILL BIT QUICK RELEASE
ACUMED
FDA UDI
Acumed LLC·10806378114045·2.8mm Quick Release Drill
HU II / HS II FIXTURE SYSTEM
FDA 510(k)
FDA Class 2
·Dental
TERUMO NEEDLE WITH LOCKING SHEATH
FDA 510(k)
FDA Class 2
·General Hospital
SMR GLENOSPHERE Ø 36MM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code KWS·July 22, 2021
2.0MM / 2.8MM THIN DRILL GUIDE
FDA Adverse Event
Injury
·ACUMED LLC·Product code HRS·April 29, 2014
8015 ALARIS SYSTEM PC UNIT
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·January 4, 2021
8015 ALARIS SYSTEM PC UNIT
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·January 4, 2021
BIODESIGN 4-LAYER TISSUE GRAFT
FDA Adverse Event
Injury
·COOK BIOTECH INC·Product code FTM·April 3, 2014
PULSE GEN MODEL 104
FDA Adverse Event
Malfunction
·CYBERONICS INC·Product code LYJ·October 22, 2012
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC., USA·Product code LFR·September 28, 2007
MEDSYTEM III INFUSION PUMP
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·February 9, 2021
8100 ALARIS PUMP MODULE
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·January 20, 2021