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

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    BIOMET 3I PATIENT SPECIFIC DENTAL ABUTMENTS-ENCODE ABUTMENTS

    FDA 510(k)
    FDA Class 2 ·Dental

    TeleRehab Software Work Station/Seat License

    FDA UDI
    SCOTTCARE CORPORATION, THE·00856298006251·The ScottCare VersaCare Cardiopulmonary Monitor...

    Tasso+ Convenience Kit

    FDA UDI
    Tasso Inc.·00860006434588·Tasso+ convenience kit allows self-collection o...

    Tasso+ Convenience Kit

    FDA UDI
    Tasso Inc.·00860006434571·Tasso+ convenience kit allows self-collection o...

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383554237·Gutta Percha Points is used to root canal filin...

    eTRAX™ Needle

    FDA UDI
    CIVCO MEDICAL INSTRUMENTS CO., INC.·10841436103357·Sterile needle, 16GA x 8cm with (7.6 tapered to...

    eTRAX™ Needle

    FDA UDI
    CIVCO MEDICAL INSTRUMENTS CO., INC.·00841436103343·Sterile needle, 16GA x 8cm with (7.6 tapered to...

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383501811·Gutta Percha Points is used to root canal filin...

    MODEL 235GE-64; MULTI PURPOSE FLEX ARRAY COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    BLAINE SCARCARE PATCH

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Complete Cervical

    FDA UDI
    Seaspine Orthopedics Corporation·10889981040444·Implant - 16x14x8mm - 6 deg

    SPECTRA WAVEWRITER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 11, 2019

    Ascendant

    FDA UDI
    Choice Spine, LP·10885862260574·

    CERVICAL IMPLANT 16X14X7MM

    FDA Adverse Event
    Injury ·THEKEN SPINE LLC·Product code ODP·May 29, 2012

    MEDALLION SYRINGE

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code FMF·May 3, 2013

    TRILOGY ALUMINA INSERT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code MRA·August 27, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 11, 2011

    UNK PERSONA TIBIA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 18, 2025

    UNKNOWN PERSONA TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 12, 2025

    UNKNOWN NEXGEN TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 13, 2025