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

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    Rondek PGA Suture (Beige or Violet)

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

    SSW CARBIDE GREAT WHITE

    FDA UDI
    Ss White Burs, Inc.·D6901806252·GREAT WHITE GOLD CARBIDE GW2 - 5 PACK

    ZenFlex

    FDA UDI
    Kerr Corporation·00195062030079·Rotary Files

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197530170·Ferreira Style Breast Retractor 180x25...

    SMITH & NEPHEW MIS HIP STEM WITH STIKTITE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REALEYE MODEL VCPS

    FDA 510(k)
    FDA Class 2 ·Radiology

    COVIDIEN

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code KNT·July 24, 2024

    COVIDIEN

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code KNT·July 24, 2024

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·January 28, 2026

    EDGE

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY VALLEYLAB, A DIVISION OF TYCO HEALTHCARE·Product code GEI·July 22, 2011

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 20, 2013

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code CBK·October 15, 2014

    SKINTACT

    FDA Adverse Event
    Injury ·LEONHARD LANG GMBH·Product code DRX·January 21, 2019

    SKINTACT

    FDA Adverse Event
    Malfunction ·LEONHARD LANG GMBH·Product code MKJ·June 19, 2019

    CAPIOX FX OXYGENATOR

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·October 9, 2019

    ROSA Brain 3.0 Application-Brain

    FDA Enforcement
    Class II ·Terminated·MEDTECH SAS·February 19, 2020

    BIOMET StageOne Hip Cement Spacer Mold with Insert, 52 MM, Silicone, Sterile, Item 431182.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·April 15, 2020

    cobas 6000 Modular Series system; Part Numbers: 1. 04745914001 cobas c 501 module; 2. 05036453001 cobas 6000 UL c 501 + Core Fix configuration; 3. 05036453692 - cobas 6000 UL + CORE CU; and 4. 05860636001 cobas 6000 c 501 (UL) V

    FDA Enforcement
    Class II ·Terminated·Roche Diagnostics Corporation·March 14, 2018