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

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    BREEZE C MODEL C (3W), BREEZE C (4W)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517563590·CoRoent Ant TLIF PEEK, 10x12x30mm 4°

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515061279·Iris Sci, str, 4 1/2" (11.5cm)

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515233928·Cushing Bayonet Fcps, insul, irrig, 2mm tip, 7 ...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694008921·3 x 4 Hole Compression T Plate

    ST AIA PACK HBA1C

    FDA 510(k)
    FDA Class 2 ·Hematology

    ADC 656 ELECTRONIC STETHOSCOPE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 30, 2025

    DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·March 7, 2017

    TRILOGY 200

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code CBK·April 30, 2013

    CAD II

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·September 19, 2014

    RASCAL

    FDA Adverse Event
    Malfunction ·ELECTRIC MOBILITY CORP.·Product code INI·May 16, 2011

    MLRY-HD LAT POR FEMORAL 8MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·November 12, 2013

    MLRY-HD LAT POR FEMORAL 8MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·November 12, 2013

    M2A-MAGNUM PF CUP 56ODX50ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·November 12, 2013

    M2A-MAGNUM 42-50MM TAPER INSERT-6

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·November 12, 2013

    M2A-MAGNUM PF CUP 56ODX50ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·November 12, 2013

    M2A-MAGNUM 42-50MM TAPER INSERT-6

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·November 12, 2013

    CIAGLIA BLUE RHINO PERCUTANEOUS TRACHEOSTOMY INTRODUCER SET WITH SHILEY

    FDA Adverse Event
    Injury ·COOK INC·Product code JOH·January 31, 2019

    Model 511 Cardio Respiratory Monitor with Oximax technology with software version 5.0

    FDA Recall
    Terminated ·CAS Medical Systems, Inc.·Product code BZQ·May 24, 2004