BEUDAMED
    13 results · 28ms · Sources: EU EUDAMED, US FDA

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    JAHN VENTILATION TUBE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902140873·Pediatric Two-Lumen Central Venous Catheterizat...

    MAXBRAID PE

    FDA UDI
    TELEFLEX INCORPORATED·04026704601615·Blue Co-braid Polyethylene Size 0 38" T-2 Needl...

    DIGORA Optime

    FDA UDI
    PaloDEx Group Oy·06430035872473·

    MAXBRAID PE

    FDA UDI
    TELEFLEX INCORPORATED·14026704601612·Blue Co-braid Polyethylene Size 0 38" T-2 Needl...

    TELEFLEX

    FDA UDI
    TELEFLEX INCORPORATED·54026704601610·Blue Co-braid Polyethylene Size 0 38" T-2 Needl...

    FLEXIMARC, MODEL CM-0.9-2-10-GG-L

    FDA 510(k)
    FDA Class 2 ·Radiology

    SV DBS BRAIN ARRAY, MODEL 1500SV-SMS64

    FDA 510(k)
    FDA Class 2 ·Radiology

    FFB WH/BL CO-BR 0 T-2 1N 38" BIOMET

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GAT·November 19, 2018

    ESSURE

    FDA Adverse Event
    Injury ·BAYER·Product code HHS·June 27, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·January 7, 2013

    DEXTRUS 4137

    FDA Adverse Event
    Other ·BIOTRONIK SE & CO. KG·Product code NVZ·November 12, 2010

    REVISION MODULAR STEM Ø16MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code LZO·June 22, 2022