18 results · 25ms · Sources: EU EUDAMED, US FDA

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Pulse Rx 2.0, Pulse Pro Rx 2.0

FDA 510(k)
FDA Class 2 ·Cardiovascular

CoRoent

FDA UDI
Nuvasive, Inc.·00887517578075·CoRoent Ant TLIF PEEK, 8x13x32mm 8°

Vanguard® SSK Knee System

FDA UDI
Biomet Orthopedics, LLC·00880304440135·

ENSITE SYSTEM, MODEL EE3000, AND ENSITE NAVX SURFACE ELECTRODE, MODEL EN0010

FDA 510(k)
FDA Class 2 ·Cardiovascular

POWDER FREE NITRILE EXAMINATION GLOVES, BLUE AND BLACK

FDA 510(k)
FDA Class 1 ·General Hospital

UPJ OCCLUSION BALLOON CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·December 6, 2021

PRECISION SPECTRA®

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 18, 2014

UNICEL® DXC 600I SYNCHRON® ACCESS® CLINICAL SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER·Product code JJE·June 21, 2013

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 28, 2011

SERIES-A STANDARD PATELLA

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·March 23, 2018

UPJ OCCLUSION BALLOON CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EYB·July 2, 2024

UPJ OCCLUSION BALLOON CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·February 28, 2022

BIOMET CRUCIATE TIBIAL TRAY

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·July 21, 2017

VANGUARD SSK TIBIAL BEARING

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·July 21, 2017

VANGUARD SSK INTERLOK FEMORAL COMPONENT

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·July 21, 2017

BIOMET SPLINED KNEE STEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·March 23, 2018

UPJ OCCLUSION BALLOON CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code EZL·July 8, 2022

UPJ OCCLUSION BALLOON CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·January 15, 2021