85 results
·
19ms
·
Sources: EU EUDAMED, US FDA
INTROSTAT LEAD INTRODUCER
FDA 510(k)
FDA Class 2
·Cardiovascular
X-CORE
FDA UDI
Nuvasive, Inc.·00887517268303·XC Mini Endcap, 14mm Parallel Round Ø12
Cohere
FDA UDI
Nuvasive, Inc.·00195377096111·COHERE ALIF Bolt, Ø6x20mm Fixation
Para-Pak CON-Trate
FDA UDI
MERIDIAN BIOSCIENCE, INC.·00840733102721·The Meridian CON-Trate System is a complete sys...
Kalitec Universal Instruments
FDA UDI
Kalitec Direct LLC·B07301K0602000·Tray base, 2"
Para-Pak CON-Trate
FDA UDI
MERIDIAN BIOSCIENCE, INC.·00840733103445·The Meridian CON-Trate System is a complete sys...
Melker Cuffed Emergency Cricothyrotomy Catheter Sets, Melker Universal Cricothyrotomy Catheter Set
FDA 510(k)
FDA Class 2
·Anesthesiology
MICROTEK MEDICAL WARMING DRAPE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Widex
FDA UDI
Widex A/S·05706069370522·Widex mind220 M2-CIC (Light beige ) RC coil
Widex
FDA UDI
Widex A/S·05706069556001·Widex mind220 M2-CIC (Dark brown ) RC coil
Widex
FDA UDI
Widex A/S·05706069370546·Widex mind220 M2-CIC (Clay brown ) RC coil
Widex
FDA UDI
Widex A/S·05706069370539·Widex mind220 M2-CIC (Dark brown ) RC coil
BD VACUTAINER® SERUM BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·May 1, 2026
ALARIS 17 INCH EXT SET W/.2MF & VLV PORT
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·February 11, 2020
ALARIS 17 INCH EXT SET W/.2MF & VLV PORT
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·February 18, 2020
BD VACUTAINER® SERUM BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·May 27, 2026
BD VACUTAINER® SERUM BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·May 18, 2026
8800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 24, 2014
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 14, 2013
OMNIPOD INSULIN PUMP
FDA Adverse Event
Malfunction
·INSULET CORPORATION·Product code LZG·December 21, 2010