31 results
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24ms
·
Sources: EU EUDAMED, US FDA
THE STRAUMANN ORTHO IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
CAL-CHEX CD PLUS
FDA 510(k)
FDA Class 2
·Hematology
RANDOX COMPLEMENT C3
FDA 510(k)
FDA Class 2
·Immunology
NAMILON POWDER
FDA UDI
AMERICAN TOOTH INDUSTRIES·D772ATI200404690·NAMILON POWDER 4 OZ SHADE 69
PYROPLAST POWDER
FDA UDI
AMERICAN TOOTH INDUSTRIES·D772ATI100404690·PYROPLAST POWDER 4 OZ SHADE 69
C & B FORMULA
FDA UDI
AMERICAN TOOTH INDUSTRIES·D772ATI400404690·C & B FORMULA 4 OZ SHADE 69
REMSTAR M SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS INC·Product code BZD·February 24, 2010
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·March 13, 2013
UNICEL® DXC 600I ACCESS® 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·April 5, 2011
PFC SIG RPF INS SZ 2.5 12.5MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC., DEPUY-RAYNHAM·Product code NJL·May 8, 2008
REMSTAR AUTO M-SERIES
FDA Adverse Event
Injury
·RESPIRONICS INC.·Product code BZD·December 3, 2010
M SERIES HEATED HUMIDIFIER
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BTT·March 26, 2009
M-SERIES HEATED HUMIDIFIER (AC)
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code BZD·March 3, 2010
REMSTAR PLUS M-SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code BZD·December 1, 2010
REMSTAR AUTO M-SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code BZD·December 30, 2010
M-SERIES HEATED HUMIDIFIER
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code BZD·June 18, 2009
REMSTAR PRO M-SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·December 22, 2010
M-SERIES (AC) HEATED HUMIDIFIER
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code BZD·November 5, 2010
BIPAP PLUS M-SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·December 17, 2010
M-SERIES (AC) HEATED HUMIDIFIER
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code BZD·January 20, 2011