BEUDAMED
    19 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.

    CULTURE COLLECTION DEVICE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    LinkSymphoKnee - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575304820·Knee femur prosthesis trial - LinkSymphoKnee Sy...

    LinkSymphoKnee - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575304660·Knee femur prosthesis trial - LinkSymphoKnee Sy...

    LinkSymphoKnee - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575304639·Knee femur prosthesis trial - LinkSymphoKnee Sy...

    LinkSymphoKnee - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575304677·Knee femur prosthesis trial - LinkSymphoKnee Sy...

    LinkSymphoKnee - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575304950·Knee femur prosthesis trial - LinkSymphoKnee Sy...

    LinkSymphoKnee - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575304691·Knee femur prosthesis trial - LinkSymphoKnee Sy...

    LinkSymphoKnee - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575304653·Knee femur prosthesis trial - LinkSymphoKnee Sy...

    LinkSymphoKnee - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575304622·Knee femur prosthesis trial - LinkSymphoKnee Sy...

    LinkSymphoKnee - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575304646·Knee femur prosthesis trial - LinkSymphoKnee Sy...

    LinkSymphoKnee - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575304615·Knee femur prosthesis trial - LinkSymphoKnee Sy...

    LinkSymphoKnee - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575304684·Knee femur prosthesis trial - LinkSymphoKnee Sy...

    TONOMETER, DIGITON

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    GE LIGHTSPEED CT750 HD (LIGHTSPEED 8.0)

    FDA 510(k)
    FDA Class 2 ·Radiology

    EPIDURAL CATHETERIZATION KIT

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC·Product code CAZ·October 1, 2010

    EPIC PLUS DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL INC., CRMD·Product code LWS·January 13, 2014

    QUATTRODE

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 14, 2012

    5.0MM TI LOCKING SCREW W/T25 STARDRIVE 56MM FOR IM NAILS

    FDA Adverse Event
    Injury ·SYNTHES MEZZOVICO·Product code HWC·May 29, 2015

    BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026