BEUDAMED
    58 results · 26ms · 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 ×

    LIFESTYLES, CONTEMPO OR PRIVATE LABEL STRAWBERRY, VANILLA, OR BANANA FLAVORED CONDOM

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

    PowerPICC SOLO

    FDA UDI
    Bard Access Systems, Inc.·00801741096273·Catheter Placement Kit

    TEWA

    FDA UDI
    asia-med Gesellschaft für Akupunkturbedarf mbH & Co. KG·04251282501723·TeWa 5CB-Type 3040 Speed Pak: coated acupunctu...

    TEWA

    FDA UDI
    asia-med GmbH·04251282509040·TeWa 5CB-Type 3040 Speed Pak: coated acupunctu...

    NiTi Archwires

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730013767·NiTi RCS Type 5 Lower 21x25 10 archwires per pack

    TruFlex

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730014733·NiTi RCS Lower 21x25 10 archwires per pack

    4WEB Medical

    FDA UDI
    4web Medical·00812998048762·

    Admiral

    FDA UDI
    Seaspine Orthopedics Corporation·10889981239398·Trial Drill Guide, 8mm

    SEALOUETTE FIBRIN SEALANT EXTENDED DROPLET APPLICATOR, MODEL TE-1

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RAPID RHINO-ANTERIOR 90MM, MODEL RR-A 90, RAPID RHINO-POSTERIOR 100MM, MODEL RR-P 100

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

    CM DRIVE IMPLANT 3.5X8

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·November 9, 2017

    CARDIOSAVE HYBRID W/ E/F PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·January 29, 2025

    OMNIPOD 5 CONTROLLER

    FDA Adverse Event
    Injury ·INSULET CORPORATION·Product code QFG·September 29, 2022

    ADVIA CENTAUR CP TROPONIN ULTRA ASSAY

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MMI·March 12, 2013

    IMHS CP ROUND IMPLAN

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPAEDICS GERMANY·Product code JDS·February 24, 2011

    LIBERTE' MONORAIL CORONARY STENT DELIVERY STENT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code MAF·February 20, 2008

    OMNIPOD 5 CONTROLLER

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code QFG·October 31, 2022

    OMNIPOD 5 CONTROLLER

    FDA Adverse Event
    Injury ·INSULET CORPORATION·Product code QFG·September 30, 2022

    OMNIPOD 5 CONTROLLER

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code QFG·September 24, 2022

    OMNIPOD 5 CONTROLLER

    FDA Adverse Event
    Injury ·INSULET CORPORATION·Product code QFG·September 30, 2022