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

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    HIGH PRESSURE SETS-400 PSI

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MICROCLAVE CLEAR CONNECTOR

    FDA Adverse Event
    Malfunction ·ICU MEDICAL, INC.·Product code FPA·June 5, 2014

    OptiBite Disposable Biopsy Forceps

    FDA UDI
    Micro-Tech (Nanjing) Co., Ltd.·06932503540360·Normal handle, Alligator, without spike, Singl...

    Osstell SmartPeg Type 69

    FDA UDI
    Osstell AB·09010522001752·ISQ Measurement Peg

    MINI NEUROLOGICAL RONGEUR

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896048102·MINI NEUROLOGICAL RONGEUR CURVED TIP

    Ear Tip ET-20 Pack/100 pcs.

    FDA UDI
    PATH medical GmbH·04260223141904·14mm mushroom ear tip

    Ear Tip ET-20 Pack/50 pcs.

    FDA UDI
    PATH medical GmbH·04260223141928·14mm mushroom ear tip

    Ear Tip ET-20 Pack/250 pcs.

    FDA UDI
    PATH medical GmbH·04260223141911·14mm mushroom ear tip

    BREG

    FDA UDI
    BREG, INC.·00672736133989·PC WAVE KNEE Y ADAPTER

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450480496·

    HS Dia.Burr,coarse,Ø4.0x95,80k

    FDA UDI
    Bien-Air Surgery SA·17630055507171·

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·November 18, 2015

    ELECSYS CORTISOL CALCHECK

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    MONARCH SPINE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VACUETTE BLOOD COLLECTION TUBES SERUM

    FDA Adverse Event
    Malfunction ·GREINER BIO-ONE NA INC.·Product code JKA·January 9, 2021

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·August 3, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·August 4, 2015

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·October 8, 2015

    EON RECHARGEABLE IPG, 16-CHANNEL

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·September 24, 2015

    SUMMIT UNIVERSAL BROACH HANDLE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code LXH·September 19, 2014