1,076 results
·
26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ZEISS 30 SL-OMNI
FDA Adverse Event
Other
·COHERENT MEDICAL LASER GRP.·Product code HQF·December 27, 1996
ENDO KIT
FDA Adverse Event
Other
·COHERANT MEDICAL LASER GRP.·Product code HQF·March 14, 1997
AMS AMBICOR
FDA Adverse Event
Injury
·PFIZER HOSP PRODUCTS GRP·Product code FHW·February 3, 1997
ULTRAPULSE CO2 LASER
FDA Adverse Event
Injury
·COHERANT, INC. MEDICAL GRP·Product code GEX·January 24, 1997
LIQUICHEK UNASSAYED CHEMISTRY CONTROL
FDA Adverse Event
Other
·BIO-RAD, DIAGNOSTICS GRP.·Product code JJY·June 16, 2011
PAINSMART IOD
FDA Adverse Event
Malfunction
·MOOG MEDICAL DEVICE GRP·Product code FRN·July 9, 2013
PAINSMART IOD
FDA Adverse Event
Malfunction
·MOOG MEDICAL DEVICE GRP·Product code FRN·July 9, 2013
PAINSMART IOD
FDA Adverse Event
Malfunction
·MOOG MEDICAL DEVICE GRP·Product code FRN·July 9, 2013
PAINSMART IOD
FDA Adverse Event
Malfunction
·MOOG MEDICAL DEVICE GRP·Product code FRN·July 9, 2013
PAINSMART IOD
FDA Adverse Event
Malfunction
·MOOG MEDICAL DEVICE GRP·Product code FRN·July 9, 2013
4000CMS
FDA Adverse Event
Malfunction
·MOOG MEDICAL DEVICE GRP·Product code FRN·July 9, 2013
PAINSMART IOD
FDA Adverse Event
Malfunction
·MOOG MEDICAL DEVICE GRP·Product code FRN·July 9, 2013
2000CMS
FDA Adverse Event
Malfunction
·MOOG MEDICAL DEVICE GRP·Product code FRN·July 9, 2013
4000CMS
FDA Adverse Event
Malfunction
·MOOG MEDICAL DEVICE GRP·Product code FRN·July 9, 2013
4000CMS
FDA Adverse Event
Malfunction
·MOOG MEDICAL DEVICE GRP·Product code FRN·July 9, 2013
PAINSMART IOD
FDA Adverse Event
Malfunction
·MOOG MEDICAL DEVICE GRP·Product code FRN·July 9, 2013
PAINSMART IOD
FDA Adverse Event
Malfunction
·MOOG MEDICAL DEVICE GRP·Product code FRN·July 9, 2013
MEDFUSION
FDA Adverse Event
Malfunction
·ST PAUL·Product code FRN·November 19, 2020
PRISMA
FDA Adverse Event
Death
·GAMBRO INDUSTRIES·Product code FJK·July 18, 2006
PRISMA
FDA Adverse Event
Death
·GAMBRO INDUSTRIES·Product code FJK·July 18, 2006