BEUDAMED
    27 results · 35ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION TO MEDRAD SPECTRIS MR INJECTOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040007952·Zirlux 16+ A2 89x17x12

    FOSTER GRANT

    FDA UDI
    FGX INTERNATIONAL INC.·00193033343098·

    SEEDNET, MODELS FP6T5, FP5T5, FP5T3

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

    TITAN POROCOAT HIP PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DANEK PLATE AND SCREW

    FDA Adverse Event
    Injury ·SOFAMOR DANEK MANUFACTURING·Product code HRS·May 19, 1999

    RENU WITH MOISTURE LOC

    FDA Adverse Event
    Injury ·BAUSCH & LOMB SOLUTIONS·Product code LPN·May 17, 2006

    IMPLANTABLE COLLAMER LENS (ICL)

    FDA Adverse Event
    Injury ·STAAR SURGICAL COMPANY·Product code QCB·August 30, 2023

    SUMMIT POR TAPER SZ6 STD OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDIC INC, 1818910·Product code LPH·June 21, 2018

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 20, 2013

    BRAVO

    FDA Adverse Event
    Malfunction ·GIVEN IMAGING LTD.·Product code FFT·February 10, 2011

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·August 15, 2014

    SUMMIT POR TAPER SZ4 HI OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDIC INC, 1818910·Product code LPH·June 20, 2018

    SUMMIT POR TAPER SZ6 HI OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDIC INC, 1818910·Product code LPH·June 1, 2018

    3 TO 1 DERMACARRIER (FOR USE WITH MESHGRAFT II TISSUE EXPANSION SYSTEM)

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL, INC.·Product code FZW·September 25, 2023

    SUMMIT POR TAPER SZ4 HI OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·September 28, 2018

    SUMMIT POR TAPER SZ7 HI OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·October 18, 2019

    SUMMIT POR TAPER SZ4 HI OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. - 8010379·Product code LPH·July 1, 2015

    PINN CAN BONE SCREW 6.5MMX15MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 14, 2018

    SUMMIT POR TAPER SZ6 STD OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 14, 2018