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

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    Trinity ELE Plus and Trinity ELE Plus Pro

    FDA 510(k)
    FDA Class 2 ·Neurology

    PPS PI

    FDA UDI
    PEROUSE MEDICAL·03661234011162·Pressure Injectable Safety Huber Needle

    Philips

    FDA UDI
    Sbo Hearing A/S·05714464002764·HEARLINK 5000 FW 1.0

    16PW - Krispy Kreme FAK - Poly White

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588015064·16PW - Krispy Kreme FAK - Poly White

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68120190600090·9mm SM HL Expanding Trial, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68120190600080·8mm SM HL Expanding Trial, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68120190600110·11mm SM HL Expanding Trial, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68120190600130·13mm SM HL Expanding Trial, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68120190600100·10mm SM HL Expanding Trial, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68120190600120·12mm SM HL Expanding Trial, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68120190600140·14mm SM HL Expanding Trial, HiJAK™ Cervical

    QUINTON Q-CATH, MODEL 000460

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ELECSYS INSULIN CALSET

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    BD¿ ABBOTT TUBE K2 EDTA (K2E) PLASTIC COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·July 19, 2018

    BLT Ø3.3MM NC, SLA® 8MM, TIZR, LOXIM

    FDA Adverse Event
    Injury ·INSTITUT STRAUMANN AG·Product code DZE·September 19, 2019

    IFUSE IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·SI-BONE, INC.·Product code OUR·June 1, 2015

    CARDIOHELP

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·January 26, 2023

    BD VENFLON¿ PRO SAFETY SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·October 22, 2019

    ARROW

    FDA Adverse Event
    Injury ·ARROW·Product code LJS·October 16, 2008

    CALYPSO

    FDA Adverse Event
    Malfunction ·ARJO HOSPITAL EQUIPMENT AB·Product code FSA·June 27, 2013