BEUDAMED
    73 results · 23ms · Sources: EU EUDAMED, US FDA

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    MODEL SR-115 PORTABLE X-RAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    ACE Surgical Supply

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950008858·ACE 1 GRAM CALCIUM SULFATE HEMIHYDRATE KIT

    Aveta Waste Management Accessory

    FDA UDI
    MEDITRINA, INC.·00850006759385·Aveta Waste Management Accessory (with cap) for...

    Face-Cradle

    FDA UDI
    MERCURY ENTERPRISES, INC.·10641043520017·

    JOBST forMen

    FDA UDI
    BSN MEDICAL, INC.·04042809663143·FOR MEN 15-20 MM HG KNEE HIGH CLOSED TOE MEDIUM...

    IV Pole Cart, M3000

    FDA UDI
    Medical Technical Products, Inc.·00850039020063·

    P102, S102 DUAL, 6", NO DP, CURBELL

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828129541·P102, S102 DUAL, 6", NO DP, CURBELL

    BREEZE SLEEPGEAR WITH DREAMSEAL

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SMARTSCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CALCIUM SULFATE HEMIHYDRATE

    FDA Adverse Event
    Malfunction ·ACE SURGICAL·Product code LYC·July 28, 2010

    ARCHITECT CA19-9XR

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code NIG·October 31, 2025

    ALINITY I CA 19-9XR REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code NIG·May 19, 2026

    11MM/130 DEG TI CANN TROCH FIXATION NAIL 400MM/LEFT-STER

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HSB·April 11, 2013

    DUAL CUT SAGITTAL BLADE

    FDA Adverse Event
    Malfunction ·STRYKER IRELAND LTD.·Product code HWE·February 28, 2011

    SWAN-GANZ THERMODILUTION VENOUS INFUSION PORT (VIP) CATHETER WITH AMC THROMBOSHI

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES, PR·Product code DYG·May 21, 2008

    ALINITY I CA 19-9XR REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code NIG·May 1, 2026

    THORACIC PACK , Model No UTTC82Y UTTC82AA-01

    FDA Enforcement
    Class II ·Ongoing·American Contract Systems Inc·March 26, 2025

    LAMITRODE S-4 LEAD KIT, 60CM LENGTH

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·March 24, 2015

    ALINITY I CA 19-9XR REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code NIG·May 14, 2026

    ALINITY I CA 19-9XR REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code NIG·December 9, 2025