BEUDAMED
    30 results · 22ms · 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 ×

    GEO 1st MTP Joint Arthrodesis Plating System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NuVasive

    FDA UDI
    Nuvasive, Inc.·00887517183309·Universal Handle, Left

    DEBAKEY TISSUE FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896059924·DEBAKEY TISSUE FORCEPS FLAT HANDLE

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180188921·SCHROEDER VULSELLUM, DOUBLE TOOTH (9 1/2") TENA...

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR32001081·Tube left f. mand. protrusion appliance

    Bradshaw Medical Inc.

    FDA UDI
    Bradshaw Medical, Inc.·00810019930096·BIT, HEX MALE 1/16" AO

    VIDAS® ESTRADIOL II

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code CHP·June 26, 2019

    AMEDICA DRUG TEST THC, COC, OPI, AMP, MET, PCP, BAR, BZO, MDMA, OXY, TCA

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    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

    VIDAS® ESTRADIOL II

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code CHP·July 23, 2019

    VIDAS® ESTRADIOL II

    FDA Adverse Event
    Injury ·BIOMERIEUX SA·Product code CHP·July 23, 2019

    BD VACUTAINER® K2 EDTA (K2E) 7.2MG BLOOD COLLECTION TUBE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·March 15, 2023

    MEDTRONIC ANEURX BIFURCATED STENT GRAFT (FLEXIBLE)

    FDA Adverse Event
    Injury ·MEDTRONIC AVE PERIPHERAL DIVISION·Product code MIH·July 3, 2002

    SHILEY CUFFLESS TRACHEOSTOMY TUBE

    FDA Adverse Event
    Malfunction ·MALLINCKRODT MEDICAL, INC.·Product code BTO·October 24, 1996

    CADD LEGACY PUMPS 6400

    FDA Adverse Event
    Injury ·ST PAUL·Product code FRN·August 30, 2022

    PROLIEVE THERMODILITATION KIT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MEQ·October 15, 2008

    AXIUM 3-D DETACHABLE COIL

    FDA Adverse Event
    Malfunction ·EV3 NEUROVASCULAR·Product code HCG·August 10, 2011

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·July 1, 2013

    MYOCARDIAL LEAD

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 8, 2013

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·June 11, 2021