5,448 results
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35ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HED-LOC™
FDA UDI
DARCO INTERNATIONAL, INC.·00609271489103·Universal
HORIZON EXPERT DOCUMENTATION
FDA Adverse Event
MCKESSON INFORMATION SOLUTIONS LLC·Product code NSX·April 1, 2010
COAGUCHEK XS SYSTEM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code GJS·February 11, 2009
UNKNWON FEMORAL HED
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·June 25, 2018
DST
FDA Adverse Event
Malfunction
·SMV INTERNATIONAL·Product code IYE·March 3, 2000
HED DDRIVER, 2.5 MM
FDA Adverse Event
Malfunction
·DEPUY MITEK·Product code HXX·April 12, 2010
NATRELLE BREAST IMPLANTS
FDA Adverse Event
Injury
·ALLERGAN·Product code FTR·March 5, 2019
TOTALCARE
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·December 20, 2010
CENTRA BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·January 15, 2013
ARJO SAF-KARY
FDA Adverse Event
Other
·ARJO MFG. CO.·Product code INM·August 15, 1997
TOTALCARE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·April 19, 2012
TAMPAX PEARL COMPAK PLASTIC
FDA Adverse Event
Malfunction
·TAMPAX·Product code HEB·November 14, 2015
SECURE 3 MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·September 26, 2012
PERSONAL BACK PLUS
FDA Adverse Event
Injury
·INVACARE CORP.·Product code IMS·March 3, 1997
TRANSTAR STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FPO·January 19, 2009
ALLEGRETTO WAVE EYE-Q
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code LZS·December 18, 2013
TOTALCARE BARIATRIC PLUS BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·August 20, 2012
FLEXTEND IS-1 BI POSITIVE FIX
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code DTB·November 9, 2006
UNKNOWN ACCOLADE STEM
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·March 18, 2024
RESTORE SENSOR
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·March 19, 2019