BEUDAMED
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    RHEIN MEDICAL

    FDA Adverse Event
    Injury ·KATENA PRODUCTS, INC·Product code HND·October 10, 2019

    RHEIN MEDICAL I/A HANDPIECE

    FDA Adverse Event
    Malfunction ·RHEIN MEDICAL INC·Product code GEI·July 12, 2002

    RHEIN

    FDA Adverse Event
    Injury ·RHEIN MEDICAL·Product code HQE·March 29, 2004

    BINKHORST TIP

    FDA Adverse Event
    Malfunction ·RHEIN MEDICAL·Product code HQE·June 24, 1994

    CONNOR WAND

    FDA Adverse Event
    Injury ·RHEIN MEDICAL·Product code HND·December 4, 1998

    FINE-NAGAHARA PHACO CHOPPER

    FDA Adverse Event
    Other ·RHEIN MEDICAL, INC.·Product code HNR·January 26, 2000

    SEIBEL CHOPPER

    FDA Adverse Event
    Injury ·RHEIN MEDICAL INC.·Product code HNQ·August 2, 2013

    GORE® CARDIOFORM SEPTAL OCCLUDER

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MLV·July 12, 2023

    NAGAHARA PHACO CHOPPER, RH DOMINANT

    FDA Adverse Event
    Malfunction ·KATENA PRODUCTS INC.·Product code HND·May 1, 2025

    UNKNOWN APEX PINS

    FDA Adverse Event
    Injury ·STRYKER GMBH·Product code JDW·July 20, 2022

    AMPLATZER SEPTAL OCCLUDER

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code MLV·April 1, 2024

    AMPLATZER SEPTAL OCCLUDER

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL·Product code MLV·April 1, 2024

    DENTAL SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·September 27, 2021

    Rheon Medical SA

    Manufacturer
    🇨🇭 Switzerland·1 Importer

    Rein medical GmbH

    Manufacturer
    🇩🇪 Germany·44 Basic UDI-DIs·172 Devices

    Suzhou Heins Medical Equipment Co.,Ltd

    Manufacturer
    🇨🇳 China·6 Basic UDI-DIs·6 Devices

    Kingsmead Service B.V.

    Authorized representative
    🇳🇱 Netherlands·243 Manufacturers·2698 Devices

    REIN MEDICAL GMBH

    FDA registration
    REIN MEDICAL GMBH·2 products·🇩🇪 Germany

    CMC Medical Devices & Drugs SL

    Authorized representative
    🇪🇸 Spain·698 Manufacturers·11260 Devices

    SINODEU 324-342

    Device
    EU MDR · Eu Md Class 1 ·Rein medical GmbH·Not intended for eu market