BEUDAMED
    27 results · 22ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    MICRORAPTOR REGENESORB Suture Anchor

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    All Poly Keel Punch Guide

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215063917·

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197081115·HEANEY needle holder, curved 21 cm,...

    CERVICAL PLATE VARIABLE SELF-DRILLING SCREW DIAM. 4X16MM (2X)

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code KWQ·November 10, 2016

    CERVICAL PLATE FIXED SELF-TAPPING SCREW DIAM. 4X14MM (2X)

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWQ·September 13, 2018

    NANOSS BONE VOID FILLER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REGENEREX TIBIAL COMPONENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MECTA C VARIABLE SELF-DRILLING SCREW DIAM. 4X18MM (2X)

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code KWQ·June 24, 2022

    CERVICAL PLATE VARIABLE SELF-TAPPING SCREW DIAM. 4X14MM (2X)

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWQ·June 8, 2018

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 17, 2014

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·July 27, 2011

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 20, 2013

    PV TRACKER GUIDE WIRE

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code DQX·May 4, 2018

    PV TRACKER GUIDE WIRE

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code DQX·May 4, 2018

    FLEXCATH ADVANCE STEERABLE SHEATH

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code DRA·May 4, 2018

    PV TRACKER GUIDE WIRE

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code DQX·May 4, 2018

    PV TRACKER GUIDE WIRE

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code DQX·May 4, 2018

    OPTILENE 6/0 (0,7) 75CM 2XDRC13 CV2 RCP

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAW·December 9, 2025

    OPTILENE 7/0 (0,5) 60CM 2XDRC8 CV2 RCP

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAW·December 9, 2025

    CERVICAL PLATE FIXED SELF-TAPPING SCREW DIAM. 4X18MM (2X)

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code KWQ·September 15, 2021