2,641 results
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33ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Verisafe
FDA UDI
Promisemed Medical Devices Inc.·00850011833988·Verifine Safety Sterile Syringes have two types...
Verisafe
FDA UDI
Promisemed Medical Devices Inc.·00850062218093·Verifine Safety Sterile Syringes have two types...
Verisafe
FDA UDI
Promisemed Medical Devices Inc.·00850062218123·Verifine Safety Sterile Syringes have two types...
Verisafe
FDA UDI
Promisemed Medical Devices Inc.·00850062218192·Verifine Safety Sterile Syringes have two types...
Verisafe
FDA UDI
Promisemed Medical Devices Inc.·00850062218116·Verifine Safety Sterile Syringes have two types...
Verisafe
FDA UDI
Promisemed Medical Devices Inc.·00850062218178·Verifine Safety Sterile Syringes have two types...
Verisafe
FDA UDI
Promisemed Medical Devices Inc.·00850062218079·Verifine Safety Sterile Syringes have two types...
UNI-CP COMPRESSION PLATE UNKNOWN
FDA Adverse Event
Injury
·NEWDEAL SAS·Product code HRS·April 11, 2018
Verisafe
FDA UDI
Promisemed Medical Devices Inc.·00850011833995·Verifine Safety Sterile Syringes have two types...
Verisafe
FDA UDI
Promisemed Medical Devices Inc.·00850062218390·Verifine Safety Sterile Syringes have two types...
Verisafe
FDA UDI
Promisemed Medical Devices Inc.·00850062218598·Verifine Safety Sterile Syringes have two types...
Verisafe
FDA UDI
Promisemed Medical Devices Inc.·00850062218406·Verifine Safety Sterile Syringes have two types...
VASOVIEW HEMOPRO 2
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code GEI·November 7, 2011
VASOVIEW HEMOPRO 2
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code GEI·November 7, 2011
VASOVIEW HEMOPRO2
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code GEI·November 7, 2011
VASOVIEW HEMOPRO 2
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code GEI·November 7, 2011
VASOVIEW HEMOPRO 2
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code GEI·November 7, 2011
VASOVIEW HEMOPRO 2
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC.·Product code GEI·November 7, 2011
VASOVIEW HEMOPRO 2
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC.·Product code GEI·November 7, 2011
ONYX AVM
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·April 26, 2022