BEUDAMED
    24 results · 24ms · Sources: EU EUDAMED, US FDA

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    SEPRAGEL SINUS

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526189775·LEVAMED ACTIVE ANKLE SUP BLACK R II

    Absolute Pro

    FDA UDI
    ABBOTT VASCULAR INC.·08717648175824·Absolute Pro Vascular Self-Expanding Stent Syst...

    Absolute Pro

    FDA UDI
    ABBOTT VASCULAR INC.·08717648175862·Absolute Pro Vascular Self-Expanding Stent Syst...

    Absolute Pro

    FDA UDI
    ABBOTT VASCULAR INC.·08717648175831·Absolute Pro Vascular Self-Expanding Stent Syst...

    Absolute Pro

    FDA UDI
    ABBOTT VASCULAR INC.·08717648175848·Absolute Pro Vascular Self-Expanding Stent Syst...

    Absolute Pro

    FDA UDI
    ABBOTT VASCULAR INC.·08717648175879·Absolute Pro Vascular Self-Expanding Stent Syst...

    Absolute Pro

    FDA UDI
    ABBOTT VASCULAR INC.·08717648175855·Absolute Pro Vascular Self-Expanding Stent Syst...

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 7, 2026

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 7, 2026

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 7, 2026

    PicoSure 532 Delivery System

    FDA UDI
    Cynosure, LLC·00841494106980·PicoSure 532 Delivery System

    MITYVAC

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    OSTEOSET BVF KIT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNKNOWN VERSASTEP

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code GCJ·June 11, 2015

    SYNERGY

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 26, 2022

    LOCKING HOLDING SLEEVE- STANDARD FOR MATRIX

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code LXH·March 20, 2013

    DUROM US ACETABULAR COMPONENT 56/50 P

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·February 24, 2011

    NATURALYTE

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·August 12, 2014

    Oridion CO2 sampling lines and water traps under the label: Omnistream CO2 Sampling Lines: OmniLine O2 Adult Part No.007609; OmniLine O2 Pediatric Part No 007610; Smart OmniLine Plus O2 Adult Part No.010177; Smart OmniLine Plus O2 Adult (package of 100 units) Part No.010213; Smart OmniLine O2 Pediatric Part No. 007606; ;Smart OmniBloc O2 Part No. 010946 Smart OmniLine Plus part No. 010172 Smart OmniLine Plus (package of 100 units) Part No 010212; Smart OmniLine Guardian O2 Part No. 012531; Smart OmniLine Guardian O2 Long Part No. 012532 OmniVentLine Set Part No. 012495

    FDA Recall
    Terminated ·Oridion Medical·Product code CCK·February 16, 2012