BEUDAMED
    54 results · 124ms · Sources: EU EUDAMED, US FDA

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    D & R PRODUCTS CO., INC.

    FDA registration
    D & R PRODUCTS CO., INC.·1 product·🇺🇸 United States

    KARL STORZ

    FDA Adverse Event
    Other ·D & R PRODUCTS CO., INC.·Product code HTT·March 28, 2006

    HENRY SCHEIN(R) 101-0913 Explorer #2 D/E. Barcode *+H658101091306*. Made in China. For professional use only. Instruments must be cleaned and sterilized prior to use. Distributed by: HENRY SCHEIN, INC. 135 Duryea Road, Melville, NY 11747 USA. This product is a dental explorer made of stainless steel packaged individually within a sleeve and containing a cardboard insert (labeling). 510 (k) exempt, Class I device, Device Listing # B057701.

    FDA Recall
    Terminated ·Hu-Friedy Mfg Co, Inc.·Product code EKB·March 29, 2004

    AMBULIFT CLASSIC

    FDA Adverse Event
    Malfunction ·MEDIBO MEDICAL PRODUCTS NV·Product code FSA·July 20, 2012

    Obelis s.a.

    Authorized representative
    🇧🇪 Belgium·546 Manufacturers·18515 Devices

    VICRYL RAP UND 45CM M0.7 USP6/0 SGLE ARMED P-1 PRIME

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·August 18, 2025

    O-ARM 1000 IMAGING SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·November 7, 2016

    ENDOWRIST

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·May 13, 2026

    PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code NEW·May 2, 2024

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·March 28, 2024

    UNKNOWN VICRYL RAPIDE SUTURE

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·March 28, 2024

    NOVOSYN VIOLET 3/0 (2) 10X60CM

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAM·June 12, 2018

    PROGAVSA SHUNTSYSTEM

    FDA Adverse Event
    Malfunction ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·June 5, 2018

    VCL CT BRD VIO 27IN 0 S/A CTX

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAM·March 18, 2021

    TECNIS IOL

    FDA Adverse Event
    Injury ·AMO PUERTO RICO MFG. INC.·Product code MFK·March 2, 2023

    PROGAV 2.0 WITH SA25 AND DISTAL CATHETER

    FDA Adverse Event
    Malfunction ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·September 20, 2018

    MONOCRYL POLIGLECAPRONE 25 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAN·March 13, 2026

    ENDOWRIST

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·May 27, 2021

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·March 21, 2024

    NUROLON NYLON SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAR·May 3, 2023