BEUDAMED
    49 results · 74ms · Sources: EU EUDAMED, US FDA

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    SAFE SNAP TB SYRINGE

    FDA Adverse Event
    Malfunction ·U.S. MEDICAL INSTRUMENTS, INC.·Product code FMF·August 12, 1996

    SAFESNAP SYRINGE

    FDA Adverse Event
    Malfunction ·U.S. MEDICAL INSTRUMENTS, INC.·Product code FMF·August 8, 1996

    SAFESNAP SYRINGE

    FDA Adverse Event
    Malfunction ·U.S. MEDICAL INSTRUMENTS, INC.·Product code FMF·August 7, 1996

    SAFE SNAP TB SYRINGE

    FDA Adverse Event
    Malfunction ·U.S. MEDICAL INSTRUMENTS, INC.·Product code FMF·August 12, 1996

    SAFE SNAP TB SYRINGE

    FDA Adverse Event
    Malfunction ·U.S. MEDICAL INSTRUMENTS, INC.·Product code FMF·August 12, 1996

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·August 11, 2017

    SUPRAMID BLACK 5/0 (1) 45CM DS16

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAR·March 3, 2017

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·June 21, 2019

    PROSPACE TITANIUM PLIF IMPL.8° 7X7X22MM

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS·Product code MAX·March 3, 2017

    MONOSYN VIOLET 3/0 (2) 70CM HS26(M) .

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAM·February 15, 2017

    DAFILON BLUE 4/0 (1.5) 45CM DS16 (M)

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAR·April 1, 2016

    MONOPLUS VIOLET 2/0 (3)70CM HS26S(M).

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code NEW·March 17, 2017

    MONOMAX VIOLET 0 (3,5) 150CM HR37S(M)DDP

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code NWJ·March 29, 2016

    SUPRAMID BLACK 5/0 (1) 45CM DS16

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAR·May 15, 2017

    PLASMAFIT PLUS 7 CUP ¿CAP SIZE 54MM H

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS·Product code KWL·June 8, 2017

    ERBOTOM ICC 350 E

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·October 7, 2016

    ERBE BICLAMP LAP FORCEPS

    FDA Adverse Event
    Other ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·April 10, 2015

    DePuy Synthes various orthopedic instruments modified by U.S. Distributors These instruments are used in various orthopedic procedures

    FDA Recall
    Terminated ·DePuy Orthopaedics, Inc.·Product code LXH·January 6, 2017

    DUROM US ACETABULAR COMPONENT 54/48 N

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·December 13, 2010

    DADE INNOVIN

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GJS·December 29, 2015