BEUDAMED
    22 results · 27ms · 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 ×

    CentriMag Circulatory Support System, CentriMag Return (Arterial) Cannula Kit, CentriMag Drainage (Venous) Cannula Kit

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377047373·RELINE-O Trial, 10mm H Pedicle L-pop

    Guide

    FDA UDI
    Treace Medical Concepts, Inc.·00810111224031·MIS Guide

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694006446·2.0mm Pilot Drill, Long, Osteopower

    ELMED INCORPORATED

    FDA UDI
    ELMED INCORPORATED·00198506062124·REPLACEMENT SEALING CAP FOR OPERATING SCOPE WIT...

    Bradshaw Medical Inc.

    FDA UDI
    Bradshaw Medical, Inc.·00810019930232·BIT, HEXALOBE 25 AO

    KENDALL SCD SEQUENTIAL COMPRESSION COMFORT SLEEVES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PINNACLE ACETABULAR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·May 27, 2021

    HAMILTON-C3

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·February 9, 2024

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 28, 2025

    ITREL 3

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code LGW·July 16, 2015

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 17, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 11, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·July 1, 2013

    AXS VECTA 074 CATH 132CM - CE

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR-CALIF·Product code QJP·July 24, 2024

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MRU·April 22, 2024

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·June 10, 2020

    UNKNOWN NEXGEN LEGACY CONSTRAINED CONDYLAR KNEE FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 4, 2025

    UNKNOWN NEXGEN LEGACY CONSTRAINED CONDYLAR KNEE ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 4, 2025