BEUDAMED
    29 results · 23ms · Sources: EU EUDAMED, US FDA

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    BENCOX II STEM, BENCOX METAL HEAD

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ArgenZ HT+ 98x25 B3

    FDA UDI
    ARGEN CORPORATION, THE·D818122099·Dental porcelain/ceramic restoration kit

    Rumex

    FDA UDI
    RUMEX INTERNATIONAL CORP.·00840159900987·Curved Vitreoretinal Scissors, 25 Ga, Tip Only

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SAFE-T-PEEL SAFETY NEEDLE/INTRODUCER, MODELS 350-300 S, 360-300'S,380-300'S,390-300'S

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ENCOR ENSPIRE SYSTM 115V

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·February 24, 2021

    PONSKY DUAL PORT FEEDING ADAPTOR, 20F

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code KNT·August 3, 2021

    PONSKY DUAL PORT FEEDING ADAPTOR, 20F

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code KNT·February 1, 2021

    PONSKY DUAL PORT FEEDING ADAPTOR, 20F

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code KNT·May 21, 2021

    PONSKY DUAL PORT FEEDING ADAPTOR, 20F

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code KNT·September 18, 2020

    BARD MAGNUM REUSABLE CORE BIOPSY INSTRUMENT

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·November 5, 2020

    PONSKY DUAL PORT FEEDING ADAPTOR, 20F

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code KNT·October 1, 2020

    ENCOR DRIVER

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·November 16, 2022

    GMK STD CEMENTED FEMUR SIZE 3 LEFT

    FDA Adverse Event
    Injury ·Product code JWH·April 29, 2015

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·May 21, 2013

    PRECISION SPECTRA®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 26, 2014

    PFC KEEL TIB TRAY CEM SZ4

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIV OF DEPUY ORTHOPAEDICS, INC.·Product code JWH·June 3, 2011

    POWERPORT M.R.I. IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, 8F

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (BASD) -3006260740·Product code LJT·July 9, 2024

    COOK TURBO-FLO HD HEMODIALYSIS CATHETER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code MPB·February 13, 2017

    ENCOR DRIVER

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·July 9, 2021