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

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    Vyntus ONE with CART, Vyntus ONE PFT only with CART, Vyntus ONE with adjustable CART, Vyntus ONE PFT only with adjustable CART

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Neuro Cochlear Implant System

    FDA UDI
    NEURELEC·03663227001822·PACKING SET, NEURO2 ZTI EXCHANGE BOX C093

    TASMIN R 18°

    FDA UDI
    SIGNUS Medizintechnik GmbH·04047844015032·The basic shape of the TASMIN R devices is a ho...

    MiniSPC Button

    FDA UDI
    APPLIED MEDICAL TECHNOLOGY, INC.·00842071150709·18F x 1.5cm MiniSPC Low Profile Suprapubic Cath...

    MiniSPC Button

    FDA UDI
    APPLIED MEDICAL TECHNOLOGY, INC.·00842071148089·18F x 1.5cm MiniSPC Low Profile Suprapubic Cath...

    SPECTRA-LOR, 10 ML PLASTIC LOSS OF RESISTANCE SYRINGE, L/S, SPECTRA-LOR, 10ML PLASTIC LOSS OF RESISTANCE SYRINGE L/L

    FDA 510(k)
    FDA Class 2 ·General Hospital

    C2000 POWERED WHEELCHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 11, 2025

    UNKNOWN ULNAR STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWI·February 23, 2018

    S5 STOCKERT CENTRIFUGAL PUMP SYSTEM

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DWA·July 15, 2011

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 21, 2013

    POLARIS ULTRA URETERAL STENT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code FAD·September 25, 2008

    UNKNOWN ULNAR STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWI·February 23, 2018

    UNKNOWN ULNAR STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWI·February 23, 2018

    QUADRA-P FEMORAL STEMS

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·November 18, 2025

    UNKNOWN ULNAR COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·February 20, 2018

    UNKNOWN ULNAR STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDB·February 23, 2018

    UNKNOWN HUMERAL STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDB·February 23, 2018

    UNKNOWN HUMERAL STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·February 23, 2018

    UNKNOWN HUMERAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDB·February 23, 2018