BEUDAMED
    10,000 results · 31ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    LRE MEDICAL GMBH

    FDA registration
    LRE MEDICAL GMBH·11 products·🇩🇪 Germany

    QUICKTEK BLOOD GLUCOSE METER

    FDA Adverse Event
    Injury ·LRE·Product code NBW·November 15, 2007

    20G Angled LRE EndoProbe® Single

    FDA UDI
    IRIDEX CORPORATION·00851089000524·

    ALINITY I STAT HIGH SENSITIVITY TROPONIN-I

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code MMI·May 2, 2024

    NATRELLE 133S TISSUE EXPANDERS

    FDA Adverse Event
    Malfunction ·ALLERGAN, INC.·Product code LCJ·September 22, 2025

    20G Angled LRE EndoProbe® Box of 6

    FDA UDI
    IRIDEX CORPORATION·00851089000517·

    ELECSYS TROPONIN T HS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code MMI·March 20, 2023

    ARCHITECT TOTAL B-HCG REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code DHA·March 28, 2023

    ALINITY C CREATININE REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code CGX·December 2, 2024

    ALINITY I FREE T4 REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code CEC·May 23, 2025

    ARCHITECT FREE T4 REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code CEC·March 13, 2025

    ALINITY I FREE T4 REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code CEC·March 13, 2025

    LRE CAPITELLAR COMP XLG/UK

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·April 21, 2016

    UNSPECIFIED HA FILLER

    FDA Adverse Event
    Injury ·GALDERMA Q-MED·Product code LMH·March 14, 2019

    LRE RAD HD 5CM MED BRGS

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWI·April 17, 2014

    ARCHITECT C4000 ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·August 20, 2019

    LRE SEGMENTAL RAD STEM 6 X 55MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDC·August 22, 2012

    DUODOPA_DUOPA

    FDA Adverse Event
    Injury ·ABBVIE MEDICAL DEVICE CENTER·Product code KNT·April 21, 2025

    ARCHITECT STAT HIGH SENSITIVITY TROPONIN-I REAGENT KIT

    FDA Adverse Event
    Malfunction ·A.I.D.D LONGFORD·Product code MMI·March 25, 2022

    Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d) C400 CORPUS II LR e) C500 CORPUS II f) C500 CORPUS II LR

    FDA Recall
    Terminated ·Permobil, Ab Arvaltsvagen 10·Product code ITI·September 1, 2017