77 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VIRTUE VENTRAL URETHRAL ELEVATION SLING SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16740826400·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674082640060·
Centaur Pedicle Screw System
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215126995·
Zavation
FDA UDI
Zavation LLC·00842166149465·8x26x40mm, 0°, MILC
ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORIES, ELECTROSURGICAL WANDS
FDA 510(k)
FDA Class 2
·Orthopedic
FREEDOM AUTOMATIC FILM PROCESSOR
FDA 510(k)
FDA Class 2
·Radiology
WAVEWRITER ALPHA
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 28, 2024
MAHURKAR CENTRAL VAS CATH
FDA Adverse Event
COVIDIEN·Product code MPB·April 24, 2013
CLARION
FDA Adverse Event
Malfunction
·ADVANCED BIONICS, LLC·Product code MCM·May 2, 2011
LIBERTE' MONORAIL CORONARY STENT DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code MAF·July 23, 2008
GLIDESHEATH
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DYB·August 7, 2019
GLIDESHEATH
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DYB·July 7, 2022
GLIDESHEATH
FDA Adverse Event
Death
·TERUMO MEDICAL CORPORATION·Product code DYB·September 6, 2023
GLIDESHEATH
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DYB·December 1, 2020
RADIFOCUS INTRODUCER
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DYB·May 19, 2022
RADIFOCUS INTRODUCER
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DYB·January 21, 2022
GLIDESHEATH
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DYB·September 28, 2023
RADIFOCUS INTRODUCER
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DYB·June 25, 2020
RADIFOCUS INTRODUCER
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DYB·June 25, 2020