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

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    RESPIRATORY BELT SENSOR, MODEL 6000S; LIMB MOVEMENT SENSOR, MODEL 3000S

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Abiomed Breethe OXY-1 System

    FDA UDI
    Breethe, Inc.·00813502013245·Tubing, Translucent Green, 1/4" x 3/8"

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001030·artVeneer life lower anteriors, UIL, A1

    XCM Biologic® Tissue Matrix

    FDA UDI
    DSM BIOMEDICAL, INC.·00812337020305·

    RINGFIX

    FDA UDI
    Stryker GmbH·00886385010052·RingFix, Ring & Foot Plate Set Tray

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·04546540429490·SCALPEL HANDLE NO. 3

    Fuji Cervical Plate System

    FDA UDI
    Altus Spine, LLC·00843210133232·Plate Holder

    PAQ.345X300X1000/EEG/001030

    FDA UDI
    AB MEDICA GROUP, S.A.·08428763007272·

    Duo Lumbar Interbody Fusion System

    FDA UDI
    SPINEOLOGY INC.·M7401001030·Duo Trial, 16mm, 8°

    Medical Facets NC

    FDA UDI
    MEDICAL FACETS NC LLC·M933MDF20010300·2.4mm Cannulated Screw, Self Drilling, Long Thr...

    SuperCable® Grip and Plate System

    FDA UDI
    Kinamed, Inc.·00818720010021·Trochanteric Grip, 4-Hole Plate

    Diamond Orthopedic, LLC

    FDA UDI
    DIAMOND ORTHOPEDIC, LLC·B551DMD2001030·2.4mm, Cannulated Screw, Self Drilling, Long T...

    HARDYDISK, NALIDIXIC ACID, 30MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    SONOACE 600 DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    BIPOLAR MACRO FORCEPS D:5/ 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 6, 2015

    BIPOLAR MARYLAND DISS.FCPS 5MM 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·March 9, 2015

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 29, 2014

    JAW INS. BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG.·Product code GEI·January 13, 2015

    TITAN INFLATABLE PENILE PROSTHESIS FAMILY

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code FHW·August 9, 2024

    ORTHOPEDIATRICS 4.0MM CANNULATED CANCELLOUS SCREW, FULL THREAD, T15, 60MM

    FDA Adverse Event
    Injury ·ORTHOPEDIATRICS, CORP·Product code HWC·January 24, 2018