BEUDAMED
    15 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    MODULAR PROTUSIO CUP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690195269·AK3 Slope Setter

    Copper Ni-Ti - Archwire

    FDA UDI
    ORMCO CORPORATION·00889989086119·COPPER NITI 35 BAF 16X22 UP LG PK10 W/STOPS

    Pro-Retractor Vertical Extension Bar

    FDA UDI
    KOROS U.S.A., INC.·10840199542267·Pro-Retractor Vertical Extension Bar (Fat Bar) 1"

    Patriot Spinal Fixation System

    FDA UDI
    VALORUS SPINE LLC·00811771032875·Crosslink Caliper

    DISPOSABLE VACUUM CURETTE

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    Disposable Sclerotherapy Needle

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024223905·

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024223899·

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024223882·

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024223875·

    ALTRX +4 NEUT 36IDX52OD

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code LPH·March 5, 2013

    MEDTRONIC SYNCHROMED 2

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code LKK·February 9, 2011

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·August 7, 2014

    FLEXCATH CONTOUR¿ STEERABLE SHEATH

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code DRA·October 7, 2024