BEUDAMED
    26 results · 22ms · Sources: EU EUDAMED, US FDA

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    CRAWFORD BIOCANALICULUS INTUBATION

    FDA 510(k)
    FDA Unclassified ·Unknown

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776187408·TC MAYO HEGAR N.H.

    CHS

    FDA UDI
    Smith & Nephew, Inc.·03596010062154·AMBI COMPRESSION HIP SCREW PLATE 6SL 140MM 140D

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780377184·Integra® Jarit® Mayo-Hegar Needle Holder, 10-1/...

    CINTAS CORPORATION

    FDA registration
    CINTAS CORPORATION·26 products·🇺🇸 United States

    TM "Soloventex" 121-142 XL

    FDA UDI
    REABILITIMED TOV·04823097718353·Women's closed-toe socks, 2nd compression class...

    TM "Soloventex" 121-142 S

    FDA UDI
    REABILITIMED TOV·04823097718322·Women's closed-toe socks, 2nd compression class...

    TM "Soloventex" 121-142 L

    FDA UDI
    REABILITIMED TOV·04823097718346·Women's closed-toe socks, 2nd compression class...

    TM "Soloventex" 121-142 XXL

    FDA UDI
    REABILITIMED TOV·04823097718360·Women's closed-toe socks, 2nd compression class...

    TM "Soloventex" 121-142 M

    FDA UDI
    REABILITIMED TOV·04823097718339·Women's closed-toe socks, 2nd compression class...

    HEARTWAY LIGHTWEIGHT POWER MOBILITY SCOOTER, S34

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    ALL SILICONE HEMATURIA CATHETER, MODELS 4861, 4862, 4863, 4864, 4865

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

    ANGEL SYSTEM WITH ASPIRATION KIT W/ ACDA

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code ORG·March 5, 2019

    ARTHREX ANGEL SYSTEM WITH ASPIRATION KIT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code ORG·May 1, 2019

    IDENTITY ADK DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWP·January 13, 2014

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·May 20, 2013

    ALARIS PUMP MODULE IV ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORPORATION·Product code FPA·May 4, 2011

    ORTHOSIS, PEDICLE, SPINAL FIXATION

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code MNI·September 25, 2015

    XIA TITANIUM 4.5 BLOCKER

    FDA Adverse Event
    Malfunction ·STRYKER SPINE-US·Product code NKB·September 3, 2020

    ACETABULAR CUP HAP SIZE 44/50

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPAEDICS LTD·Product code NXT·April 24, 2019