188 results
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25ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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CEDIA BUPRENORPHINE ASSAY
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Leksell Stereotactic System
FDA UDI
Elekta Solutions AB·07340201502488·Curved Front Piece
BiomarC®
FDA UDI
Carbon Medical Technologies, Inc.·00858015005660·Preloaded Tribell Carbon Tissue Marker - Distal...
Myo/Wire II
FDA UDI
A & E MEDICAL CORPORATION·10841291101246·SS Suture, 7 per sleeve
neoWave LS
FDA UDI
XENIX MEDICAL LLC·00818345024113·Paddle Shaver, 16mm
InTess Lumbar Cage
FDA UDI
Kalitec Direct LLC·B07312K0103160·Shaver, Closed, 16mm
COOLTOUCH VARIA ND:YAG LASER SYSTEM; COOLTOUCH VARIA-II ND:YAG LASER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MERETEK UBT_LITE BREATH TEST FOR H. PYLORI
FDA 510(k)
FDA Class 1
·Microbiology
HT70 VENTILATOR
FDA Adverse Event
Malfunction
·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·April 3, 2013
PENUMBRA COIL 400
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code HCG·February 15, 2011
INVISALIGN
FDA Adverse Event
Injury
·ALIGN TECHNOLOGY, INC.·Product code NXC·May 8, 2008
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 2, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026