BEUDAMED
    30 results · 21ms · Sources: EU EUDAMED, US FDA

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    Acuity 85 (Oprifocon A) Rigid Gas Permeable Contact Lens

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Paltop

    FDA UDI
    PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108695458·Dynamic Dental Implant Ø3.75mm L10mm

    Guide Pin 2.7 x 100mm w Olive

    FDA UDI
    Osteocentric Technologies, Inc.·00816950029325·Guide Pin 2.7 x 100mm Olive

    INTREPED, Intraosseous Fusion Device

    FDA UDI
    Auxano Medical LLC·00850055649262·INTREPED Tray System

    Stimulator, Electrical, Implantable, For Incontinence

    FDA Pre-Market Approval
    FDA Class 3 ·VIRTIS SACRAL NEUROMODULATION SYSTEM

    NA

    FDA UDI
    Biedermann Motech GmbH & Co. KG·04250869602914·MOSS 100 Ti Head, Standard Polyaxial, rod syste...

    NA

    FDA UDI
    Biedermann Motech GmbH & Co. KG·04250869610490·MOSS VRS Ti Polyaxial Reduction Head

    NA

    FDA UDI
    Biedermann Motech GmbH & Co. KG·04250869628419·MOSS VRS MIS Ti polyaxial long head extended tabs

    MINIMALLY INVASIVE DEFORMITY CORRECTION (MID-C) SYSTEM

    FDA Adverse Event
    Malfunction ·APIFIX LTD.·Product code QGP·July 8, 2024

    MID-C 125

    FDA Adverse Event
    Malfunction ·APIFIX LTD.·Product code QGP·March 27, 2024

    MINIMALLY INVASIVE DEFORMITY CORRECTION (MID-C) SYSTEM

    FDA Adverse Event
    Malfunction ·APIFIX LTD.·Product code QGP·October 8, 2024

    MASTER CLASSIC 5K LOW SPEED HANDPIECE, 20K LOW SPEED HANDPIECE, TM5 LOW SPEED HANDPIECE AND TM20 LOW SPEED HANDPIECE

    FDA 510(k)
    FDA Class 1 ·Dental

    MOBIVISION

    FDA 510(k)
    FDA Class 2 ·Radiology

    MOSS VRS

    FDA Adverse Event
    Injury ·BIEDERMANN MOTECH GMBH & CO. KG·Product code NKB·February 12, 2025

    OPTILOCK IMPLANTABLE ACCESS PORT, MODELS #1700-01, 1700-02, 1700-03, 1700-04 AND 1700-05

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CROSS-LINK-CLAMP F/R Ø6 PREASSMBL TAN DB

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code NKB·June 14, 2013

    ZOOM

    FDA Adverse Event
    Malfunction ·EXTERNAL MANUFACTURER·Product code KRG·July 20, 2011

    GLOBAL SHD END PEG GLEN 44

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWT·September 18, 2008

    OSTEO-SITE BONE BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNW·July 18, 2019

    OSTEO-SITE BONE BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNW·June 17, 2019