10,000 results
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36ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Snowden-Pencer
FDA UDI
STERIS CORPORATION·10885403458705·Snowden-Pencer MIS ERGONOMIC MODULAR JOHANN GRA...
Snowden-Pencer
FDA UDI
STERIS CORPORATION·10885403458699·Snowden-Pencer MIS ERGONOMIC MODULAR JOHANN GRA...
JSA'S REPROCESSED COMPRESSION SLEEVE DEVICES
FDA 510(k)
FDA Class 2
·Cardiovascular
JSA REPROCESSED COMPRESSION SLEEVE DEVICES
FDA 510(k)
FDA Class 2
·Cardiovascular
REAGENT RED BLOOD CELLS 0.8% RESOLVE PANEL C
FDA Adverse Event
Malfunction
·ORTHO CLINICAL DIAGNOSTICS·Product code KSZ·December 13, 2016
PANOCELL
FDA Adverse Event
Malfunction
·IMMUCOR, INC.·Product code KSZ·January 5, 2007
1056600-2006-00530
FDA Adverse Event
Malfunction
·Product code KSZ·December 5, 2006
RESOLVE PANEL B
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 5, 2006
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·August 11, 2014
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HRS·August 11, 2014
GALILEO
FDA Adverse Event
Malfunction
·IMMUCOR·Product code KSZ·July 20, 2007
ID CORE XT
FDA Adverse Event
Malfunction
·PROGENIKA BIOPHARMA S.A.·Product code PEP·December 9, 2019
PANOCELL-16
FDA Adverse Event
Malfunction
·IMMUCOR·Product code KSZ·November 6, 2009
GAMMACLONE ANTI-D (MONOCLONAL BLEND)
FDA Adverse Event
Malfunction
·GAMMA BIOLOGICALS, INC.·Product code KSZ·August 4, 2006
GNS-F4 CARD
FDA Adverse Event
Malfunction
·VITEK SYSTEMS, INC.·Product code JSA·March 16, 1994
DEFENSE BLOOD STANDARD SYSTEM (DBSS)
FDA Adverse Event
Injury
·DOD/DMLSS/DBSS·Product code MMH·November 10, 2004
ECHO LUMENA
FDA Adverse Event
Malfunction
·IMMUCOR, INC.·Product code KSZ·October 31, 2024
ECHO LUMENA
FDA Adverse Event
Malfunction
·IMMUCOR, INC.·Product code KSZ·November 5, 2024
SEARCH-CYTE TCS 0.8%
FDA Adverse Event
Malfunction
·MEDION GRIFOLS DIAGNOSTICS AG,·Product code QHT·May 9, 2025
Culture Media, Antibiotic Assay
FDA classification
FDA Class 1
·Culture Media, Antibiotic Assay