66 results · 28ms · Sources: EU EUDAMED, US FDA

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C-Stem AMT LE Prosthesis

FDA 510(k)
FDA Class 2 ·Orthopedic

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526781733·LUMBAMED FACET 3 POINT SILVER VI

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526743694·ACHIMED ACHILLES SUPP SILVER VI

BD Calibrated Disposable Inoculating Loops, Blue

FDA UDI
BECTON, DICKINSON AND COMPANY·00382902202165·BD Calibrated Disposable Inoculating Loops, Blu...

APEX PS Knee

FDA UDI
Omni Life Science, Inc.·00841690113119·PS Insert, Size 2 x 16mm

TALOS° HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B1676220216150·

TALOS° HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B1676220216000·

TALOS° HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B1676220216070·

Coral

FDA UDI
Seaspine Orthopedics Corporation·10889981029210·Fixed X-Conn 16mm

4K UHD Camera System

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

GENOSYL MV-1000

FDA 510(k)
FDA Class 2 ·Anesthesiology

GS

FDA Adverse Event
Malfunction ·LEONHARD LANG GMBH·Product code MKJ·June 28, 2022

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·August 12, 2025

BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·December 8, 2023

BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·December 8, 2023

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·November 3, 2014

SYNCHROMED II

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·August 16, 2011

DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR

FDA Adverse Event
Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·July 11, 2013

BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code FPA·December 1, 2023

BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

FDA Adverse Event
Injury ·BECTON, DICKINSON AND COMPANY (BD)·Product code FPA·February 16, 2024