BEUDAMED
    32 results · 21ms · 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 ×

    Endopath Electrosurgery Probe Plus II

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

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486009458·MCK BASEPLATE TEMPLATE (SIZE 8 LM/RL)

    LeMaitre Embolectomy Catheter

    FDA UDI
    Lemaitre Vascular, Inc.·00840663100569·2F 80 cm LeMaitre Embolectomy Catheter, eIFU

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694032650·1.7mm Drill/Countersink Combo, Long, Manual

    Monza Cervical Plate System

    FDA UDI
    Altus Spine, LLC·B41711601281·28mm Cervical Plate, 1 Level

    LeMaitre Embolectomy Catheter

    FDA UDI
    Lemaitre Vascular, Inc.·00840663100453·2F 80 cm LeMaitre Embolectomy Catheter

    WAVEWRITER ALPHA? 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·March 24, 2026

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694068123·Cannulated 1.7mm Drill/Countersink Combo, Long,...

    CLEARBLUE EASY DIGITAL PREGNANCY TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TRINITY ACETABULAR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ONE TOUCH PROFILE

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·September 23, 2002

    ONE TOUCH PROFILE

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·September 20, 2002

    5.0MM TI LOCKING SCREW 32MM- FOR IM NAILS-STERILE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·June 10, 2013

    COLLEAGUE 3 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 16, 2008

    VASOVIEW HEMOPRO 2

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·June 2, 2011

    LeMaitre Embolectomy Catheter 2F Single Lumen, Balloon Volume 0.05 ml , Length 80 cm Latex Product Number: 1601-28

    FDA Recall
    Terminated ·Lemaitre Vascular, Inc.·Product code DXE·February 7, 2005

    VENTED HUMIDIFICATION CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·September 28, 2016

    GALAXY G3 MINI 2MM X 4CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·June 16, 2021

    GALAXY G3 5MM X 15CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·June 16, 2021

    GALAXY G3 MINI 3MM X 8CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·June 16, 2021