BEUDAMED
    27 results · 27ms · Sources: EU EUDAMED, US FDA

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    MOTEX POLYISOPRENE POWDER-FREE SURGICAL GLOVES MODEL # 6412(6432) AND # 6512(6532)

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    RUSCH

    FDA UDI
    TELEFLEX INCORPORATED·04026704300839·Green Non-Latex Robertazzi Nasopharyngeal Airwa...

    Stryker

    FDA UDI
    Provision·B504OM51201231260·

    NA

    FDA UDI
    STRYKER CORPORATION·04546540466952·12.6mm x 10.4mm Boring Tool

    NA

    FDA UDI
    STRYKER CORPORATION·04546540466907·12.6mm x 10.4mm Boring Tool

    AMEDITECH IMMUTEST HCG PREGANCY TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TROPHON CHEMICAL INDICATOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·August 9, 2023

    T:SLIM G5 SYSTEM

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code OYC·March 27, 2019

    ABBOTT CLINICAL CHEMISTRY CREATINE KINASE

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code CGS·October 24, 2007

    I-STAT TROPONIN (CTNI) CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE, INC.·Product code MMI·February 14, 2012

    PRESTO UP&UP BGMS

    FDA Adverse Event
    Injury ·AGAMATRIX, INC.·Product code NBW·January 26, 2016

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·May 21, 2013

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 20, 2008

    DUROM US ACETABULAR COMPONENT 56/50 P

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·June 6, 2011

    I-STAT TROPONIN (CTNI) CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE INC.·Product code MMI·January 19, 2012

    G7 LONGEVITY NEUTRAL 36MM F

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·January 31, 2024

    CEMENT CENTRALIZER/PLUG

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code JDI·April 21, 2026

    CATH-LAB SHEATH INTRO SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DYB·February 12, 2016

    SCULPTRA

    FDA Adverse Event
    GLOBAL PHARMACOVIGILANCE AND EPIDEMIOLOGY/SANOFI-AVENTIS·Product code LMH·December 21, 2009