BEUDAMED
    30 results · 23ms · Sources: EU EUDAMED, US FDA

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    PRO GEAR N95 PARTICULATE FILTER RESPIRATOR & SURGICAL MASK, REGULAR SIZE MODEL RP CERIES

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

    Marienfeld Superior

    FDA UDI
    Paul Marienfeld GmbH & Co. KG·04250317329097·

    Oticon

    FDA UDI
    Oticon A/S·05707131158376·HIT, RITE TC

    ARGEDENT B YELLOW PF

    FDA UDI
    ARGEN CORPORATION, THE·D818102092·Gold based noble metal

    SYMPHONY

    FDA UDI
    Medos International Sàrl·10705034527468·SYMPHONY OCT SYSTEM DUAL DIAMETER ROD COBALT CH...

    SYMPHONY

    FDA UDI
    Medos International Sàrl·10705034527475·SYMPHONY OCT SYSTEM DUAL DIAMETER ROD COBALT CH...

    COVERIS

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030CS1020920·Trial, 13 x 18mm, 3° Lordotic, 8mm

    SPIRA®-A Integrated

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030SAZ1020920·SPIRA®-A Integrated,Trial, 30x42mm, 25° Lordoti...

    CAAS QVA 3D, CAAS QCA 3D

    FDA 510(k)
    FDA Class 2 ·Radiology

    CORVUS RADIATION THERAPY PLANNING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    POLYMER FASTENERS

    FDA Adverse Event
    Injury ·INNOVASIVE DEVICES·Product code MBI·September 7, 2001

    POLYMER FASTENERS

    FDA Adverse Event
    Injury ·INNOVASIVE DEVICES·Product code MBI·September 7, 2001

    POLYMER FASTENERS

    FDA Adverse Event
    Injury ·INNOVASIVE DEVICES·Product code MBI·September 7, 2001

    POLYMER FASTENERS

    FDA Adverse Event
    Injury ·INNOVASIVE DEVICES·Product code MBI·September 7, 2001

    POLYMER FASTENERS

    FDA Adverse Event
    INNOVASIVE DEVICES·Product code MBI·September 7, 2001

    SYRINGE 50ML LL CONVENIENCE TRAY EUROPE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·September 2, 2021

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·April 23, 2013

    MAXCEM ELITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code MZW·September 19, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 19, 2011

    BD VACUTAINER® ECLIPSE¿ BLOOD COLLECTION NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FMI·October 3, 2024