BEUDAMED
    41 results · 37ms · Sources: EU EUDAMED, US FDA

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    ENCORE SHOULDER PRIMARY HUMERAL STEM, MODEL 500-00, ENCORE SHOULDER HUMERAL HEAD, MODEL 520-38

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SW

    FDA UDI
    SW SAFETY SOLUTIONS INC.·00616489004028·PowerChem Neoprene Exam Gloves, Small

    iDuo® Patella Trial

    FDA UDI
    Conformis, Inc.·00850268007361·iDuo® 32mm Patella Trial Reusable Instrument

    InTess Lumbar Cage

    FDA UDI
    Kalitec Direct LLC·B07312K0104020·Caddie, Large, 30mm

    TiWAVE L Lumbar Cage System

    FDA UDI
    Kalitec Direct LLC·B07323K0104020·Caddie, Large, 30mm

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707065661·INTRAORAL ELASTICS 2,5 oz 5/16" blue

    Azur Pure Helical

    FDA UDI
    Microvention, Inc.·00810170018121·Azur

    SMOOTH-FLO CIRCUIT

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SCREENERS PHENCYCLIDINE (PCP) TEST, DRUGSCREEN DIP PHENCYCLIDINE (PCP) TEST

    FDA 510(k)
    FDA Unclassified ·Unknown

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523153374·Tesera X Cage, 40mm x 22mm x 8mm, Convex 0°

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523153411·Tesera X Cage, 40mm x 22mm x 12mm, Convex 0°

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523153459·Tesera X Cage, 40mm x 22mm x 16mm, Convex 0°

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523153473·Tesera X Cage, 40mm x 22mm x 18mm, Convex 0°

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523153398·Tesera X Cage, 40mm x 22mm x 10mm, Convex 0°

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523153435·Tesera X Cage, 40mm x 22mm x 14mm, Convex 0°

    AVISTA MRI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 1, 2024

    NEOPUFF INFANT RESUSCITATOR

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTL·April 20, 2011

    EMAX2PLUS

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·October 1, 2015

    MYO/PUNCH ROTATING SURGICAL PUNCH

    FDA Adverse Event
    Malfunction ·ALTO DEVELOPMENT CORP·Product code LRY·November 1, 2013

    EMAX 2 MOTOR

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·June 6, 2015