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

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    X-SERIES INTEGRAL LATERALIZED HIP COMPONENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481114090·LOCATOR R-Tx Abutment for 3.4mm External Hex Im...

    Ultracryl

    FDA UDI
    Ortho Organizers, Inc.·00190707000400·ULTRACRYL II POWDER

    BUSCH®, BNA®

    FDA UDI
    BUSCH & CO. GmbH & Co. KG·D8120305011·Diamond, cone flat, medium grit

    neoWave LS

    FDA UDI
    XENIX MEDICAL LLC·00818345027961·Lumbar Inserter, PLIF, 7-10H

    InTess Lumbar Cage

    FDA UDI
    Kalitec Direct LLC·B07312K0105010·Implant Inserter, 11-13mm, Sleeved

    Holder, Needle, Micro, Jacobson/catch round-handle 18cm tip 0.8mm

    FDA UDI
    Geister Medizintechnik GmbH·04057034007235·Holder, Needle, Micro, Jacobson/catch round-...

    ELECTROSURGICAL GENERATOR, MODEL S1

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

    N PROTEIN STANDARD UY CALIBRATOR

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Kaliec Special

    FDA UDI
    Kalitec Direct LLC·B073DRK0300010·Probe, 1.75" Egg, Steffee Long Str Imp Crimson

    ENDOSKELETON® TL

    FDA UDI
    TITAN SPINE, LLC·00191375052005·Retractor Perforated, Tray, Inner Tray

    ENDOSKELETON®

    FDA UDI
    TITAN SPINE, LLC·00191375051756·Perforated, Upper, Inner Tray

    GOMCO

    FDA UDI
    Allied Medical, LLC·00026072002322·501 CIRC. CLAMP, CHILD, 1.6

    ENDOSKELETON® DPK

    FDA UDI
    TITAN SPINE, LLC·00191375051794·Perforated, Upper, Inner Tray

    SPIN-LOC SUTURE ANCHOR SYSTEM FG-0302-01,FG-0305-01

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ELMED INCORPORATED

    FDA UDI
    ELMED INCORPORATED·00198506074578·TENSION ADJUSTMENT NUT FOR GOMCO CIRCUMCISION C...

    BOOMERANG PEEK FUSION DEVICE

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code MQP·January 14, 2011

    AMBIT PCA PUMP

    FDA Adverse Event
    Death ·SUMMIT MEDICAL PRODUCT, INC·Product code MEA·March 26, 2013

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 9, 2011

    PD2000 ADVISORY

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORP·Product code MKJ·April 16, 2008