49 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MIDAS TOUCH BLUE NITRILE EXAMINATION GLOVES-POWDER FREE
FDA 510(k)
FDA Class 1
·General Hospital
Probe Tip 'small' PT-S 5pack
FDA UDI
PATH medical GmbH·04260223142864·
CURE LP
FDA UDI
MEDITECH SPINE, LLC·B167900001450·
Golden Isles Pedicle Screw System
FDA UDI
Intelivation, LLC·G079C2520001450·Curved Ti Rod, 145mm
PedFlex Flexible Nailing System
FDA UDI
ORTHOPEDIATRICS CORP.·00841132119471·ø4.5mm Flexible IM Nail Cap (2 Each)
USB Cable
FDA UDI
GLOBAL INSTRUMENTATION, LLC·90815187020115·ECG Module USB Cable (3 meters)
CURE LP
FDA UDI
MEDITECH SPINE, LLC·B167S1900001450·
CURE LP
FDA UDI
SpineArt SA·07640270060699·ANTERIOR LUMBAR PLATE L45
PedFlex Flexible Nailing System
FDA UDI
ORTHOPEDIATRICS CORP.·00841132198193·Ø4.5 MM FLEXIBLE IM NAIL CAP (2 EACH)
INSET 30
FDA Adverse Event
Malfunction
·UNOMEDICAL UM-D·Product code FPA·March 31, 2026
INSET 30
FDA Adverse Event
Malfunction
·UNOMEDICAL UM-D·Product code FPA·March 31, 2026
INSET 30
FDA Adverse Event
Malfunction
·UNOMEDICAL UM-D·Product code FPA·March 31, 2026
MEDTRONIC EXTENSION PASSER TUNNELING SYSTEM (38 CM), MODEL 3555-38; MEDTRONIC EXTENSION PASSER TUNNELING SYSTEM (60 CM),
FDA 510(k)
FDA Class 2
·Neurology
POSITUBE
FDA 510(k)
FDA Class 2
·Anesthesiology
MERIT CUSTOM KIT
FDA Adverse Event
Malfunction
·MERIT MEDICAL SYSTEMS, INC.·Product code FMF·March 8, 2013
PERFORMANCE PRO AMBULANCE COT
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code INK·February 3, 2011
UNK
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·February 19, 2008
XPERT EV, MODEL GXEV-100N-10; GENEXPERT DX SYSTEM, MODELS P/N 900-0144, 900-0145, 900-0146, 900-0065
FDA 510(k)
FDA Class 2
·Microbiology
PANTANAIL DEVICE - UNSPECIFIED
FDA Adverse Event
Injury
·NEWDEAL SAS·Product code HSB·January 30, 2018
AUTOSOFT 30
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·August 9, 2024