16 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AMSure Hydrophilic Intermittent Catheter
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741814450·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674181445060·
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X1814450·18mm H x 14mm W x 45mm L x 0 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X181445120·18mm H x 14mm W x 45mm L x 12 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L181445120·18mm H x 14mm W x 45mm L XLIF Trial 12 degree L...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X18144580·18mm H x 14mm W x 45mm L x 8 degrees XLIF
Regatta Lateral System
FDA UDI
Seaspine Orthopedics Corporation·10889981158491·Lateral Implant, 18mm x 14mm x 45mm, 15 Deg
Regatta Lateral System
FDA UDI
Seaspine Orthopedics Corporation·10889981158484·Lateral Implant, 18mm x 14mm x 45mm, 10 Deg
Regatta Lateral System
FDA UDI
Seaspine Orthopedics Corporation·10889981158477·Lateral Implant, 18mm x 14mm x 45mm, 0 Deg
FORA COMFORTSCAN EAR THERMOMETER, MODELS TD-1261A; TD-1261B
FDA 510(k)
FDA Class 2
·General Hospital
VITAL SIGNS MONITOR-VSM 6000 SERIES
FDA 510(k)
FDA Class 2
·Cardiovascular
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 17, 2014
STEALTHSTATION S7 SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·July 5, 2011
LEAD EXTRACTION EVOLUTION MECHANICAL DILATOR SHEATH SET
FDA Adverse Event
Injury
·COOK VASCULAR INC.·Product code DRE·June 14, 2013
EPIQ 7C ULTRASOUND CHINA LOCAL
FDA Adverse Event
Malfunction
·PHILIPS ULTRASOUND (SHANGHAI) CO., LTD·Product code IYN·June 2, 2023