54 results
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23ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SURGIQUEST ANCHORPORT SIL KIT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Cattell T-Tube
FDA UDI
C. R. Bard, Inc.·00801741050459·Cattell T-Tube, X-Ray Opaque Rubber, 16 Fr
Photodynamic Bone Stabilization Procedure Pack
FDA UDI
ILLUMINOSS MEDICAL, INC.·USSL1100180·Photodynamic Bone Stabilization Procedure Pack
Photodynamic Bone Stabilization Procedure Pack
FDA UDI
ILLUMINOSS MEDICAL, INC.·M986USSL11001800·Photodynamic Bone Stabilization Procedure Pack
COOLEY COARCTATION CLAMP
FDA UDI
SONTEC INSTRUMENTS, INC.·B09921001800·COOLEY COARCTATION CLAMP CURVED JAW STRAIGHT SHANK
COOLEY COARCTATION CLAMP
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896091337·COOLEY COARCTATION CLAMP CURVED TIP STRAIGHT SHANK
Photodynamic Bone Stabilization System
FDA UDI
ILLUMINOSS MEDICAL, INC.·M986US11001800·11mmx180mm Photodynamic Bone Stabilization LED ...
TRANSANAL ENDOSCOPIC MICROSURGERY (TEM) COMBINATION SYSTEM AND INSTRUMENT SET, INSTRUMENT SET FOR THE TRANSANAL ENDOSCOP
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
REPROCESSED TROCARS, MODEL B5LT AND CB5LT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Widex
FDA UDI
Widex A/S·05706069305074·RC4 version 1 (Fashion grey, no bat )
CAPSUREFIX NOVUS LEAD MRI SURESCAN
FDA Adverse Event
Injury
·MPRI·Product code DTB·May 2, 2025
EVERA MRI XT DR SURESCAN
FDA Adverse Event
Injury
·MEDTRONIC EUROPE SARL·Product code LWS·November 6, 2025
COBALT¿ DR MRI SURESCAN¿
FDA Adverse Event
Injury
·MEDTRONIC EUROPE SARL·Product code LWS·May 20, 2024
VIVA¿ QUAD XT CRT-D
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code NIK·October 9, 2025
VIVA¿ QUAD XT CRT-D
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code NIK·October 9, 2025
CAPSUREFIX NOVUS LEAD MRI SURESCAN
FDA Adverse Event
Malfunction
·MPRI·Product code DTB·June 16, 2025
TRANSTAR STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FPO·April 29, 2013
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·September 18, 2014
TERUMO ADVANCED PERFUSION SYSTEM 1
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·May 16, 2011
UNKNOWN BEACON NEEDLE
FDA Adverse Event
Injury
·COVIDIEN LP BARRX·Product code FCG·July 20, 2022