BEUDAMED
    13 results · 26ms · Sources: EU EUDAMED, US FDA

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    FLEXI-Q DV AND DVR AUTO-INJECTORS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MAXCUT CARBIDE BUR (10/pk) FGSS 331

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D77811114671·MAXCUT CARBIDE BUR (10/pk) Shape: Pear; Size: 3...

    Surgical Instrument

    FDA UDI
    Jeil Medical Corporation·08800089447091·

    MicroSelectron Digital

    FDA UDI
    Nucletron B.V.·08717213033702·Coupling Treatment Tube for 5F Flexibles (7)

    Summa Orthopaedics System Surgical Instrument

    FDA UDI
    Jeil Medical Corporation·08800089466252·

    ROSS EMBRACE PUMP SET

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    JIE+HONG MEDICAL SURGICAL GOWNS - STERILE, JIE+HONG MEDICAL SURGICAL GOWNS - NON STERILE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    VENOUS ARTERIAL BLOOD MANAGEMENT PROTECTION KIT

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code DQO·March 12, 2008

    TRUWAVE DISPOSABLE PRESSURE TRANSDUCER W/VAMP KIT

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code DRS·July 21, 2008

    TRAUMA STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM DE MEXICO S DE RL DE CV·Product code FPO·May 3, 2013

    ASR ACETABULAR IMPLANT 62

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·May 13, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 14, 2008

    INLIVEN CRT-P, Model Numbers: a) V284 b) V285 c) W274 d) W275 (added 7/15/2021)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·July 21, 2021