49 results · 21ms · Sources: EU EUDAMED, 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