421 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Prosurg
FDA UDI
PROSURG INC·00851545007609·Neoscope Diagnostic Cystoscope
NA
FDA UDI
Southmedic Incorporated·10620974001642·Divided Nasal Cannula Adult with 7 ft O2 tube a...
ELECTRA 1600C AUTOMATIC COAGULATION ANALYZER
FDA Adverse Event
Other
·MEDICAL LABORATORY AUTOMATION·Product code GKP·January 22, 1998
PRESTIGE SMART SYSTEM GLUCOSE CONTROL LOW
FDA Adverse Event
Malfunction
·*·Product code CFR·September 26, 2001
ELECTRA 1000C
FDA Adverse Event
Injury
·MEDICAL LABORATORY AUTOMATION·Product code GKP·October 1, 1997
ELECTRA 1000C AUTOMATIC COAGULATION TIMER
FDA Adverse Event
Other
·MEDICAL LABORATORY AUTOMATION, INC.·Product code GKP·December 11, 1996
CLINICOMP CIS AND FMRD SYSTEM
FDA Adverse Event
Malfunction
·CLINICOMP INTL.·Product code HEL·June 4, 1998
UNSPECIFIED PUMP
FDA Adverse Event
Malfunction
·ICU MEDICAL COSTA RICA LTD.·Product code FRN·August 10, 2024
ELECTRA 1400C
FDA Adverse Event
Other
·MEDICAL LABORATORY AUTOMATION, INC.·Product code GKP·May 12, 1997
UNSPECIFIED PLUM 360 INFUSION PUMP
FDA Adverse Event
Malfunction
·ICU MEDICAL COSTA RICA LTD.·Product code FRN·August 8, 2024
LIFECARE PCA-3 INFUSION PUMP
FDA Adverse Event
Malfunction
·HOSPIRA·Product code MEA·May 5, 2005
SMART CONTROL NITINOL STENT SYSTEM
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code NIO·September 17, 2014
VOYAGER NC CORONARY DILATATION CATHETER
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code LOX·March 18, 2011
DILATOR
FDA Adverse Event
Injury
·COOK INC·Product code DRE·July 21, 2021
QUANTIFERON
FDA Adverse Event
Malfunction
·CELLESTIS LIMITED·Product code NCD·April 9, 2013
QUANTIFERON®-TB GOLD PLUS
FDA Adverse Event
Malfunction
·QIAGEN SCIENCES LLC·Product code NCD·October 27, 2025
QUANTIFERON
FDA Adverse Event
Malfunction
·CELLESTIS LIMITED·Product code NCD·April 9, 2013
QUANTIFERONQ
FDA Adverse Event
Malfunction
·CELLESTIS LIMITED·Product code NCD·April 9, 2013
QUANTIFERON
FDA Adverse Event
Malfunction
·CELLESTIS LIMITED·Product code NCD·April 9, 2013
QUANTIFERON
FDA Adverse Event
Malfunction
·CELLESTIS LIMITED·Product code NCD·April 9, 2013