23 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AVD INTIMAX (TM) BILIARY CATHETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756964456·STROKE DRAPE PACK
ZAVATION
FDA UDI
Zavation LLC·00842166151567·WHITNEY 13mmx15mm , 0deg , 06mm
Rampart One Lumbar Interbody Fusion System
FDA UDI
SPINEOLOGY INC.·M7404910006·Fixed Angle Drill Tip
Life Instruments
FDA UDI
Life Instrument Corporation·M93079100061R0·Frazier Suction Tube 6 FR Rigid
Life Instruments
FDA UDI
Life Instrument Corporation·M930791000610·Frazier Suction Tube 6FR 7" from bend
Life Instruments
FDA UDI
Life Instrument Corporation·M93079100061C0·Frazier Suction Tube 6FR 7" from bend
neoWave C
FDA UDI
XENIX MEDICAL LLC·00840493415024·Rasp, Universal
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0100060·Tray Insert, Lumbar Screws, 10 x 10 Assembly
OIS SYMPHONY IMAGE MANAGMENT SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
DRAINAGE CATHETER OR FOLEY CATHETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Life Instruments
FDA UDI
Life Instrument Corporation·M93079100061LR0·Lighted Suction Tube 6 Fr Right Side
Life Instruments
FDA UDI
Life Instrument Corporation·M93079100061LL0·Lighted Suction Tube 6 Fr Left Side
LONG NAIL KIT R1.5, TI, LEFT GAMMA3 10X260MM X 12
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·September 6, 2012
NA
FDA UDI
Zimmer, Inc.·00889024065482·
VITALITY 2
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 11, 2013
2800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 10, 2010
ENDOTAK RELIANCE
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVY·July 2, 2014
XRL RELEASE TOOL
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code MQP·August 24, 2021
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·December 11, 2024