BEUDAMED
    90 results · 28ms · Sources: EU EUDAMED, US FDA

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    RPM Reinforced PTFE Mesh

    FDA 510(k)
    FDA Class 2 ·Dental

    Key Surgical K-Wires and Steinmann Pins

    FDA UDI
    KEY SURGICAL, INC.·00849771015697·Steinmann Pins, Single trocar threaded, 3/32-in...

    MONARCH III IOL DELIVERY SYSTEM; MONARCH III P CATRIDGE; MONARCH III HANDPIECE (H4)

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    JOSTRA QUADROX D DIFFUSION MEMBRANE OXYGENATOR WITH BIOLINE COATING, MODEL BE-HMOD 2000, BEQ-HMOD 2030

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEPUY ASR XL FEM IMP SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·October 15, 2014

    R3

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPAEDICS, LTD.·Product code NXT·June 17, 2013

    X-STOP IPD SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SPINE LLC.·Product code NQO·July 22, 2011

    AMPLATZ EXTRA-STIFF SUPPORT WIRE GUIDE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQX·April 15, 2021

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code DQX·July 2, 2024

    BENTSON STRAIGHT FIXED CORE WIRE GUIDE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQX·August 12, 2024

    AMPLATZ EXTRA-STIFF SUPPORT WIRE GUIDE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQX·April 25, 2022

    SAFE-T-J AMPLATZ EXTRA-STIFF SUPPORT WIRE GUIDE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQX·May 3, 2024

    BENTSON STRAIGHT FIXED CORE WIRE GUIDE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQX·June 4, 2024

    SAFE-T-J AMPLATZ EXTRA-STIFF SUPPORT WIRE GUIDE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQX·September 1, 2022

    BENTSON STRAIGHT FIXED CORE WIRE GUIDE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQX·October 8, 2024

    LUNDERQUIST-RING TORQUE WIRE GUIDE

    FDA Adverse Event
    Injury ·COOK INC·Product code DQX·September 28, 2021

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code KWA·July 11, 2012

    ARTICULEZE M HEAD 36MM +8.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code JDI·July 11, 2012

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code KWA·July 11, 2012

    SAFE-T-J ROSEN CATHETER EXCHANGE WIRE GUIDE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQX·October 7, 2022