62 results · 23ms · Sources: EU EUDAMED, 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