755 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
LULLABY TM WARMER
FDA 510(k)
FDA Class 2
·General Hospital
LARGE CANNULATED SCREWS
FDA UDI
Smith & Nephew, Inc.·03596010063809·6.5MM UNIVERSAL CANNULATED SCREW 25MM
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X1216250·12mm H x 16mm W x 25mm L x 0 degrees XLIF
Meridian
FDA UDI
Seaspine Orthopedics Corporation·10889981265755·Trial, 39mm x 27mm x 16mm, 25 Deg
Cup Forceps
FDA UDI
ELLIQUENCE, LLC·00846338002381·
Meridian
FDA UDI
Seaspine Orthopedics Corporation·10889981246518·Interbody, 39mm x 27mm X 16mm, 25 Deg
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X12162580·12mm H x 16mm W x 25mm L x 8 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L121625120·12mm H x 16mm W x 25mm L XLIF Trial 12 degree L...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X121625120·12mm H x 16mm W x 25mm L x 12 degrees XLIF
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311216250·
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321216250·
Best Medical International
FDA UDI
BEST MEDICAL INTERNATIONAL, INC.·00841365119941·
COHEN CROSSOVER CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
ELECSYS HSV-1 IGG IMMUNOASSAY ELECSYS PRECICONTROL HSV
FDA 510(k)
FDA Class 2
·Microbiology
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 12, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 11, 2024
BIPAP A40
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 9, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 6, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 13, 2024
IDENTITY XL DR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC. CRMD·Product code DXY·January 13, 2014