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

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    KODAK T-MAT L FILM SO-387

    FDA 510(k)
    FDA Class 1 ·Radiology

    TELEFLEX

    FDA UDI
    TELEFLEX INCORPORATED·14026704735317·Blue Polypropylene Monofilament Size 0 two TC-4...

    T-TYPE D-KAT, R-TYPE D-KAT

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    IMMULITE 2500 AUTOMATED IMMUNOASSAY ANALYZER

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TENDRIL STS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVN·December 17, 2021

    DURATA STS OPTIM PASSIVE FIXATION, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVY·December 17, 2021

    OPTIBOND XTR

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code KLE·May 27, 2014

    VASOVIEW HEMOPRO 2

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·October 26, 2012

    LCS PFJ TROCHLEAR COMP SM+ RT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code NJL·September 9, 2010

    DEK BL MF 0 TC-43 2N 48" BSC

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GAW·June 14, 2022

    ABSORBABLE SUTURES

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code NON·October 30, 2025