BEUDAMED
    29 results · 31ms · Sources: EU EUDAMED, US FDA

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    MOJAVE CATARACT EXTRACTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    SCANLAN®

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159008890·Micro Clamp

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575407538·Orthopaedic implant inserter/extractor, reusabl...

    O-RING PROSTHETIC ATTACHMENT

    FDA 510(k)
    FDA Class 2 ·Dental

    RESPONDER 3000

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    TENDRIL SDX LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVN·October 29, 2025

    HEYER-SCHULTE SALINE-FILLED MAMMARY PROSTHESIS, 325 CC

    FDA Adverse Event
    Injury ·V. MUELLER DIV. BAXTER HEALTHCARE CORP.·Product code FWM·October 7, 1994

    HEYER-SCHULTE SALINE-FILLED MAMMARY PROSTHESIS

    FDA Adverse Event
    Injury ·V. MUELLER DIV. BAXTER HEALTHCARE CORP.·Product code FWM·October 7, 1994

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·July 21, 2016

    SALINE-FILLED MAMMARY PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR CORP.·Product code FWM·October 7, 1994

    JAW INS.BIP.MACRO FORCEPS D: 5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG TUTTLINGEN 78532·Product code GEI·December 12, 2014

    BIPOLAR MACRO FORCEPS D:5/ 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 6, 2015

    JAW INS. BIP. MARYLAND DISS. FCPS 5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·January 14, 2015

    BIPOLAR MARYLAND DISS.FCPS 5MM 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·March 9, 2015

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 29, 2014

    JAW INS. BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG.·Product code GEI·January 13, 2015

    MARYLAND GSP.FORCEPS FEN.5/310MM HF CON.

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·February 19, 2014

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·October 25, 2016

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·May 10, 2016