31 results
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24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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JUD custom fit condom
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
OsteoMed
FDA UDI
OSTEOMED LLC·00845694027175·2.4mm X 14mm Cannulated Headless Screw
OsteoMed
FDA UDI
OSTEOMED LLC·00845694068826·Cannulated 2.4 x 14mm Headless Screw Sterile Qty 5
CRYOSTAT
FDA 510(k)
FDA Unclassified
·Unknown
ELIA B2-GLYCOPROTEIN I IGA IMMUNOASSAY
FDA 510(k)
FDA Class 2
·Immunology
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·August 6, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·August 6, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·August 6, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·October 17, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·November 9, 2018
ROSA ONE
FDA Adverse Event
Injury
·MEDTECH SA·Product code HAW·January 11, 2019
COBAS E411 RACK SYSTEM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JLW·August 8, 2013
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code NAY·January 21, 2019
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·December 21, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·November 15, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·November 15, 2018
FREESTYLE
FDA Adverse Event
Malfunction
·Product code NBW·July 31, 2012
SCRW,2.4X8MM CANCELOUS LOCKING
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code HRS·June 17, 2013
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 22, 2011
HS III PROXIMAL SEAL SYSTEM 3.8 MM
FDA Adverse Event
Injury
·MAQUET CARDIOVASCULAR, LLC·Product code DXC·October 10, 2014