22 results · 34ms · Sources: EU EUDAMED, US FDA

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COBE SMARXT OPTIMIN SURFACE MODIFIED HOLLOW FIBER MEMBRANE OXYGENATOR

FDA 510(k)
FDA Class 2 ·Cardiovascular

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012672·PedFuse Remind LES, Quad, 7.0mm x 80mm

SONOMA

FDA UDI
FGX INTERNATIONAL INC.·00193033496374·

Navagio

FDA UDI
Kalitec Direct LLC·B07330K0134080·Trial, TLIF, 27L OB STR 7Deg, 8mm

Navagio

FDA UDI
Kalitec Direct LLC·B07330K0134100·Trial, TLIF, 27L OB STR 7Deg, 10mm

VIVA

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

BIOFIND

FDA 510(k)
FDA Class 2 ·Neurology

M2A-38 CUP NON FLARED SZ 54MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 20, 2013

ANT-CER 2 LVL PLATE ASSY, 40MM

FDA Adverse Event
Malfunction ·ZIMMER SPINE·Product code KWQ·February 3, 2011

ENTRUST AT

FDA Adverse Event
Injury ·MEDTRONIC MED REL, INC.·Product code LWS·March 10, 2008

ACT ARTIC E1 HIP BRG 28X54MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWY·May 30, 2019

CER BIOLOXD MOD HD 28MM -3 NK

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LZO·May 30, 2019

G7 OSSEOTI MULTIHOLE 66MM I

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·May 30, 2019

SERIES A PATELLA

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·November 29, 2017

REGENEREX TIBIAL TRAY

FDA Adverse Event
Injury ·.·Product code MBH·November 29, 2017

VANGUARD FEMORAL COMPONENT

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·November 29, 2017

MAXIM FINNED STEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·November 29, 2017

ACCESS® 2 IMMUNOASSAY CLINICAL SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code DHA·January 7, 2012

VANGUARD PS OPEN BOX FEMORAL POROUS COAT/ BOND COAT 62.5MM RIGHT

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·November 2, 2017

RGX 3 PEG SER A PATELLA 34MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code MBH·July 10, 2017