BEUDAMED
    20 results · 24ms · Sources: EU EUDAMED, US FDA

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    Cellbrick Knee Spacer

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Symmetry Weitlaner-Beckmann

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482061459·Symmetry® Retractor, Weitlaner-Beckmann, Hinged...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A243024150·24mm H x 30mm W x 24mm L x 15 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A243024120·24mm H x 30mm W x 24mm L x 12 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A24302480·24mm H x 30mm W x 24mm L x 8 degrees ALIF

    MiniSPC Button

    FDA UDI
    APPLIED MEDICAL TECHNOLOGY, INC.·00842071152802·24F x 3.0cm MiniSPC Low Profile Suprapubic Cath...

    C2 CryoBalloon Catheter (Pear), C2 CryoBalloon Catheter (Standard), C2 CryoBalloon Controller, C2 CryoBalloon Foot Pedal, C2 CryoBalloon Cartridge

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CAS-One Liver

    FDA 510(k)
    FDA Class 2 ·Neurology

    G7 VIVACIT-E

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 11, 2026

    TRILOGY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 11, 2026

    TRILOGY

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code LPH·March 11, 2026

    Z1 HIP SYSTEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWY·March 11, 2026

    G7 OSSEOTI ACETABULAR SHELL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 11, 2026

    COROX OTW 75-UP STEROID

    FDA Adverse Event
    Malfunction ·BIOTRONIK GMBH AND CO·Product code MRM·November 20, 2008

    DURATA STS OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 11, 2011

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·July 23, 2013

    SAPIEN 3 TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·February 20, 2026

    SAPIEN 3 TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·February 17, 2026

    MACROLYTE Premie Dispersive Electrode, REF 440-2400, CONMED CORPORATION. The device is applied to the patient during electrosurgical procedures to provide a path for RF current to leave the patient and return to the generator.

    FDA Recall
    Terminated ·ConMed Corporation·Product code GEI·May 8, 2014

    Direct Drive Clip Applier CA090, indicated for ligation of tubular structures or vessels in laparoscopic and general surgical procedures. Distributed individually and in kits.

    FDA Enforcement
    Class II ·Terminated·Applied Medical Resources Corp·May 18, 2016