BEUDAMED
    30 results · 22ms · Sources: EU EUDAMED, US FDA

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    SURGIMESH WN

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040067390·UPPER LEFT SINGLE BUCCAL TUBE,

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X0614450·6mm H x 14mm W x 45mm L x 0 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X061445120·6mm H x 14mm W x 45mm L x 12 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X06144580·6mm H x 14mm W x 45mm L x 8 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L061445120·6mm H x 14mm W x 45mm XLIF Trial 12 degree Lord...

    SMILIE PC

    FDA 510(k)
    FDA Class 1 ·Dental

    ETEST CEFDITOREN FOR S. PNEUMONIAE AND H. INFLUENZAE

    FDA 510(k)
    FDA Class 2 ·Microbiology

    MERSILENE POLYESTER FIBER SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·March 17, 2020

    OMEGA-21 VERTEBRAL FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·BIOMET SPAIN, S.L.·Product code MNH·February 21, 2020

    ROD, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·March 26, 2019

    XLD 110V L.A. NEW

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·April 10, 2013

    STRATA 2, ADJUSTABLE VALVE, REGULAR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROSURGERY·Product code JXG·March 16, 2011

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·September 4, 2014

    ILIAC SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·October 16, 2019

    PEDICLE SCREW, UNKNOWN TYPE OR SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·August 30, 2021

    UNKNOWN LUMBAR IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MAX·April 11, 2022

    CLOSURE TOP UNSPECIFIED

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code NKB·April 20, 2021

    CLOSURE TOP UNSPECIFIED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·April 20, 2021