24 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SCANDIUS TRITIS TIBIAL ACL RECONSTRUCTION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Prodigy No Coding Blood Glucose Test Strips
FDA UDI
Prodigy Diabetes Care, LLC·00384840528109·1 Vial of Prodigy No Coding Blood Glucose Test ...
JOBST forMen
FDA UDI
BSN MEDICAL, INC.·04042809846256·FOR MEN 20-30 MM HG KNEE HIGH CLOSED TOE LARGE ...
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450253083·
COBRASCAN CR-1 FILMLESS
FDA 510(k)
FDA Class 2
·Radiology
ANA 3000 SM NON GAMMA 2 MODIFIED SPHERICAL DENTAL ALLOY
FDA 510(k)
FDA Class 2
·Dental
SLEEPEASY
FDA Adverse Event
Injury
·RESPIRONICS INC.·Product code BZD·April 12, 2012
REMSTAR PLUS M-SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code BZD·May 6, 2010
REMSTAR M SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code BZD·November 25, 2009
M-SERIES DC POWER SUPPLY
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·May 25, 2012
SPECTRA WAVEWRITER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 11, 2021
AVALUS AORTIC TISSUE VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code LWR·June 23, 2020
COGNIS
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·April 11, 2013
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·March 15, 2011
UNIPOLAR
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC., ORTHOPAEDIC DIV.·Product code KWY·May 27, 2008
REMSTAR PLUS M-SERIES
FDA Adverse Event
Death
·RESPIRONICS, INC.·Product code BZD·March 16, 2012
REMSTAR M SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS INC·Product code BZD·February 24, 2010
REMSTAR PLUS M
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code BZD·May 21, 2010
REMSTAR PLUS M-SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code BZD·December 1, 2010
REMSTAR PLUS M-SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code BZD·May 26, 2011