62 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Beddr
FDA UDI
Beddr·00857796008013·
Beddr
FDA UDI
Beddr·00857796008020·
Beddr 200 System
FDA 510(k)
FDA Class 2
·Cardiovascular
*
FDA Adverse Event
Other
·*·Product code FRN·August 16, 1999
*
FDA Adverse Event
Other
·*·Product code KQZ·November 17, 2004
PEDICLE SCREW, PLATE
FDA Adverse Event
Injury
·ACROMED CORP.·Product code MCV·April 5, 1996
MEDTRONIC STRATAMR VALVE AND SHUBT
FDA Adverse Event
Injury
·MEDTRONIC·Product code JXG·February 6, 2018
STYLE 168 MAMM IMPLANTS
FDA Adverse Event
Injury
·MCGHAN MED CORP·Product code FWM·February 6, 2009
VANTA
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·August 10, 2022
LGN XLPE DISHED ISRT SZ 3-4 15MM
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JWH·June 11, 2025
LABOR/DELIVERY/RECOVERY BED LDR-600
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
BED RED D-DIMER WHOLE BLOOD AGGLUTINATION ASSAY
FDA 510(k)
FDA Class 2
·Hematology
STERIS BED OR
FDA Adverse Event
Other
·STERIS CO.·Product code FQO·April 13, 2007
UNK SALINE IMPLANT
FDA Adverse Event
Malfunction
·ALLERGAN (COSTA RICA)·Product code FWM·June 20, 2018
SIEMENS BI-PLANE IMAGING SYSTEM
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE GMBH·Product code IZI·March 29, 2021
NITI-S PYLORIC & DUODENAL UNCOVERED STENT
FDA Adverse Event
Death
·TAEWOONG MEDICAL CO., LTD·Product code MUM·January 27, 2015
HIGH-SPEED AND LOW SPEED BURS
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC.·Product code EQJ·August 8, 2008
SOCLEAN
FDA Adverse Event
Injury
·SOCLEAN, INC.·Product code LRJ·September 14, 2020
LASERSCOPE
FDA Adverse Event
Other
·LYRA·Product code GEX·April 12, 2006
LPS DISTAL FEM COMP XXSM RT
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JWH·June 1, 2023