BEUDAMED
    20 results · 23ms · 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.

    EXMOOR SUCTION CLEARANCE KIT

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

    BRAUN Silk Expert Pro 3

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

    SPEC MODEL M-31

    FDA 510(k)
    FDA Class 2 ·Radiology

    BD VACUTAINER® URINE COLLECTION STRAW

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code KDT·November 7, 2017

    120 ML BD VACUTAINER® PLASTIC URINE COLLECTION CUP

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code KDT·December 1, 2017

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNS·June 7, 2006

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNS·June 7, 2006

    BD VACUTAINER® PLUS PLASTIC TRANSPORT KIT FOR UA CHEMISTRY URINE TESTING

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code KDT·November 27, 2017

    120 ML BD VACUTAINER® PLASTIC URINE COLLECTION CUP

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code KDT·December 5, 2017

    120 ML BD VACUTAINER® PLASTIC URINE COLLECTION CUP

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code KDT·December 5, 2017

    120 ML BD VACUTAINER® PLASTIC URINE COLLECTION CUP

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code KDT·December 1, 2017

    BD VACUTAINER® PLASTIC URINE COLLECTION CUP

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code KDT·December 1, 2017

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNS·June 7, 2006

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GEO·June 19, 2006

    120 ML BD VACUTAINER® PLASTIC URINE COLLECTION CUP

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code KDT·December 1, 2017

    ASR ACETABULAR CUPS 58

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·March 5, 2013

    CONCERTO CRT-D DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NIK·February 15, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 7, 2014

    PROSTHESIS, HIP, SEMI-CONSTRAINED, UNCEMENTED, METAL/POLYMER, NON-POROUS, CALICU

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MEH·October 15, 2025

    Accolade TMZF Plus Hip Stem: Catalog # 3020-0537 Accolate d TMZF Hip Stem # 5 Catalog #6020-3535 Accolade 132 Size 3.5 Catalog # 6021-0230 Accolade Plus TMZF Hip Stem #2 Catalog # 6021-0335 Accolade Plus TMZF Hip Stem #3 Catalog #3021-0435 Accolade TMZF Hip Stem #4 Catalog # 6021-0435 Accolade Plus TMZF Hip Stem #4 Catalog #6021-2530 Accolade (127 deg) Size 2.5 Accolade (127 deg) Size 2.5 Catalog # 6021-4535 Accolade (127 DEG) Size 4.5 K994366; k023105; K032300 Manufactured by " Stryker Ireland, Carrigtwohill Industrial Estate Carrington County Cork, Ireland The subject hip stem is a single-use device intended for the reconstruction of the head and neck of the femoral joint. This hip stem is intended for primary reconstruction of the proximal femur or revision total hip arthroplasty.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code ISL·March 1, 2011