19 results
·
31ms
·
Sources: EU EUDAMED, US FDA
THORA-CATH TROCAR-TYPE CHEST DRAINAGE TUBE
FDA 510(k)
FDA Class 2
·General Hospital
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209117048·
Alcohol Well, 8.5mm
FDA UDI
KATALYST SURGICAL LLC·00840096207378·Alcohol Well, 8.5mm
InQwire Super Stiff Guide Wire (IQSS32180J3); InQwire Super Stiff Guide Wire (IQSS35F260S); InQwire Super Stiff Guide Wire (IQSS35F150S); InQwire Super Stiff Guide Wire (IQSS35F100S); InQwire Super Stiff Guide Wire (IQSS35F80S); InQwire Super Stiff Guide Wire (IQSS35F180S)
FDA 510(k)
FDA Class 2
·Cardiovascular
EXPLOR MODULAR RADIAL HEAD REPLACEMENT DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 22, 2014
MICRO RECIPROCATING SAW
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS KALAMAZOO·Product code ERL·October 29, 2012
STARCLOSE SE VASCULAR CLOSURE SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code MGB·September 29, 2010
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·July 26, 2019
VIDAS® ANALYZER
FDA Adverse Event
Malfunction
·BIOMERIEUX ITALIA S.P.A.·Product code JJE·October 27, 2021
VIDAS® ANALYZER
FDA Adverse Event
Malfunction
·BIOMERIEUX ITALIA S.P.A.·Product code JJE·October 27, 2021
VIDAS® ANALYZER
FDA Adverse Event
Malfunction
·BIOMERIEUX ITALIA S.P.A.·Product code JJE·October 27, 2021
VIDAS® ANALYZER
FDA Adverse Event
Malfunction
·BIOMERIEUX ITALIA S.P.A.·Product code JJE·October 27, 2021
VIDAS® ANALYZER
FDA Adverse Event
Malfunction
·BIOMERIEUX ITALIA S.P.A.·Product code JJE·October 27, 2021
VIDAS® ANALYZER
FDA Adverse Event
Malfunction
·BIOMERIEUX ITALIA S.P.A.·Product code JJE·October 27, 2021
VIDAS® ANALYZER
FDA Adverse Event
Malfunction
·BIOMERIEUX ITALIA S.P.A.·Product code JJE·October 27, 2021
VIDAS® ANALYZER
FDA Adverse Event
Malfunction
·BIOMERIEUX ITALIA S.P.A.·Product code JJE·June 3, 2021
2.7MM/3.5MM TI VA-LCP POSTLAT DHP/9H/LT/153MM-XLNG-STER
FDA Adverse Event
Injury
·SYNTHES RARON·Product code HRS·March 1, 2017
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·March 1, 2017