BEUDAMED
    59 results · 38ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION TO ERA 300 DUAL CHAMBER PACING SYSTEM ANALYZER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Aligned Medical Solutions

    FDA UDI
    Aligned Medical Solutions·B09800336130·Laparotomy/C-Section Extras Pack

    Baltic Denture System BDLoad

    FDA UDI
    Merz Dental GmbH·D7091033613·Baltic Denture System BDLoad BDLoad ↓ Mm6 PLSEu...

    SOFT PLUG ABSORBABLE PLUG-SA

    FDA 510(k)
    FDA Unclassified ·Unknown

    3.0.T SIGNA VH/I (T/R) BODY IMAGING COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    BD ULTRA-FINE¿ PRO PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·September 10, 2022

    MGRM KNEE BALANCER HEIGHT GDE

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LXH·April 3, 2013

    STEALTHSTATION TREON TREATMENT GUIDANCE SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·February 11, 2011

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·April 24, 2008

    PROGREAT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·May 7, 2026

    PROGREAT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·May 7, 2026

    PROGREAT

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQO·April 10, 2026

    PROGREAT

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQO·May 7, 2026

    Daig Livewire Steerable, Product Number 401915; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026

    PROGREAT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·May 26, 2026

    PROGREAT

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQO·July 28, 2025

    PROGREAT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·July 30, 2025

    PROGREAT

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQO·August 9, 2024

    PROGREAT CATHETER

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQO·October 15, 2024

    PROGREAT CATHETER

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DQO·December 11, 2023