21 results
·
38ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
DAN MONOPOLAR LAP ACCESSORIES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
INSPECTRA TISSUE SPECTROMETER SYSTEM (INSPECTRA), MODEL 325
FDA 510(k)
FDA Class 2
·Cardiovascular
OPTIMA MX
FDA 510(k)
FDA Class 1
·Dental
BIPAP AUTO M-SERIES
FDA Adverse Event
Death
·RESPIRONICS, INC·Product code BZD·July 11, 2012
BIPAP AUTO SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 9, 2022
BIPAP AUTO SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 14, 2022
BIPAP AUTO BIFLEX
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 14, 2022
BIPAP AUTO SERIES ASSY
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 31, 2022
BIPAP AUTO SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 14, 2022
BIPAP AUTO SERIES ASSY
FDA Adverse Event
Malfunction
·RESPIRONICS, INC·Product code BZD·March 31, 2022
BIPAP AUTO SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 9, 2022
BIPAP AUTO SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 9, 2022
BIPAP AUTO SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 9, 2022
BIPAP AUTO SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 31, 2022
FLEXTEND
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVN·April 11, 2013
ASR ACETABULAR CUPS 50
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·April 7, 2011
FENESTRATED MARYLAND BIPOLAR INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC.·Product code GEI·May 27, 2008
BIPAP AUTO M-SERIES
FDA Adverse Event
Other
·RESPIRONICS INC.·Product code BZD·June 8, 2012
BIPAP AUTO M-SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·May 20, 2011
REMSTAR BIPAP AUTO M-SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·August 27, 2010