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

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    G-IVF G5 SERIES

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    PMMA disc

    FDA UDI
    Dentsply International Inc.·D00180811160·

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014609645·BERCHTOLD 5.25" DELUXE GEL

    VECTRA (INTELECT) EPR ULTRASOUND

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    PASCO MIC AND MIC/ID PANELS INCLUSION OF ESBL CONFIRMATORY TEST

    FDA 510(k)
    FDA Class 2 ·Microbiology

    CADD MEDICATION CASSETTE

    FDA Adverse Event
    Malfunction ·NULL·Product code FPA·February 4, 2022

    DRUG ELUTING PERMANENT RIGHT VENTRICULAR (RV) OR RIGHT ATRIAL (RA) PACEMAKER ELE

    FDA Adverse Event
    Injury ·MPRI·Product code NVN·April 26, 2013

    PROMETRA PROGRAMMABLE PUMP

    FDA Adverse Event
    Injury ·FLOWONIX MEDICAL INC.·Product code LKK·August 29, 2014

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS, INNOVATION CTR - SILICON VALLEY·Product code GEX·April 14, 2011

    PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code KRO·October 15, 2025

    PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code KRO·April 23, 2026

    LGN PRSFT STEM 10MMX220MM STRT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·October 19, 2017

    CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS THAN 30 DAYS

    FDA Adverse Event
    Injury ·COOK INC·Product code FOZ·August 22, 2022

    CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS THAN 30 DAYS

    FDA Adverse Event
    Injury ·COOK INC·Product code FOZ·August 22, 2022

    TRIPLE LUMEN POLYURETHANE CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·July 3, 2018

    TRIPLE LUMEN POLYURETHANE CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·July 3, 2018

    TRIPLE LUMEN POLYURETHANE CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·June 25, 2018

    Catheter, intravascular, therapeutic, short-term less than 30 days

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FOZ·November 10, 2022

    LEGION HK HINGE KNEE SYSTEM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code KRO·March 15, 2025

    1820334-2022-00399

    FDA Adverse Event
    Injury ·COOK INC·Product code LJS·March 16, 2022