35 results
·
31ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Closed System Transfer Device
FDA 510(k)
FDA Class 2
·General Hospital
Dornier MedTech
FDA UDI
Dornier MedTech GmbH·04049958004025·Medilas H35 Holmium Laser with wired footswitch
Puget Sound Energy - 18 Metal
FDA UDI
Certified Safety Manufacturing, Inc.·00766588014692·Puget Sound Energy - 18 Metal
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450157619·
EXPERIENCE®
FDA UDI
Gc Orthodontics America Inc.·D78820146000201·EXP SL TUBE MBT 018LR6-20T 0A 0OF HK
EXPERIENCE®
FDA UDI
Gc Orthodontics America Inc.·D78820146000101·EXPERIENCE SL BTUBE ROTH 018/LR6-25T 4OF
EXPERIENCE®
FDA UDI
Gc Orthodontics America Inc.·D788201460S0201·EXM MBT 018LR6 -20T 0A 0OF HK S
ZAVATION TAP
FDA UDI
Zavation LLC·00197157021436·MIS Tap 6.0MM
VIDAS H. PYLORI IGG (HPY) ASSAY, MODEL 30 192
FDA 510(k)
FDA Class 1
·Microbiology
OCO DENTAL IMPLANT
FDA 510(k)
FDA Class 2
·Dental
HEARTWARE® VENTRICULAR ASSIST SYSTEM
FDA Adverse Event
Injury
·HEARTWARE, INC·Product code DSQ·January 31, 2014
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 29, 2025
S.M.A.R.T. NITINOL STENT SYSTEM
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code FGE·April 16, 2014
UNKNOWN BARRX
FDA Adverse Event
Injury
·COVIDIEN LP BARRX·Product code GEI·March 24, 2020
MULTI-LINK RX VISION CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code MAF·October 16, 2008
STENOSCOP
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 26, 2013
IAB: 8 FR - 30 CC
FDA Adverse Event
Malfunction
·ARROW INTL., INC.·Product code DSP·August 3, 2011
ANCURE ENDOGRAFT (FORMERLY EVT ENDOGRAFT)
FDA Adverse Event
Injury
·GUIDANT ENDOVASCULAR SOLUTIONS·Product code MIH·February 17, 2015
VALIANT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·November 3, 2014
TALENT TAA
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·November 3, 2014