BEUDAMED
    6,151 results · 19ms · Sources: EU EUDAMED, US FDA

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    RENUVION

    FDA Adverse Event
    Injury ·APYX MEDICAL CORPORATION·Product code GEI·September 20, 2021

    Radiology Software For Referral Of Findings Related To Fibrotic Lung Disease.

    FDA classification
    FDA Class 2 ·Radiology Software For Referral Of Findings Related To Fibrotic Lung Disease.

    TWO ONE TWO NEW YORK, INC.

    FDA registration
    TWO ONE TWO NEW YORK, INC.·6 products·🇺🇸 United States

    AWOS ANGIOGRAPHIC WORKSTATION

    FDA 510(k)
    FDA Class 2 ·Radiology

    Two B srl

    FDA registration
    Two B srl·2 products·🇮🇹 Italy

    OWO IMAGING LLC

    FDA registration
    OWO IMAGING LLC·1 product·🇺🇸 United States

    KINGS TWO DENTAL SUPPLY

    FDA registration
    KINGS TWO DENTAL SUPPLY·1 product·🇺🇸 United States

    TWO-HANDS CO., LTD

    FDA registration
    TWO-HANDS CO., LTD·1 product·🇰🇷 South Korea

    QKO (TM) AMYLASE B-HA

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    MICROVAC®

    FDA UDI
    PMT CORPORATION·00650551037996·ULTRA MALLEABLE SURGICAL SUCTION - WITHOUT WIRE

    MICROVAC®

    FDA UDI
    PMT CORPORATION·00650551037958·ULTRA MALLEABLE SURGICAL SUCTION - WITHOUT WIRE

    MICROVAC®

    FDA UDI
    PMT CORPORATION·00650551037910·ULTRA MALLEABLE SURGICAL SUCTION - WITHOUT WIRE

    212NY

    FDA UDI
    Two One Two New York, Inc.·G33527000L1·IIJA COMPLIANT DISPOSABLE ISOLATION GOWN LEVEL ...

    212NY

    FDA UDI
    Two One Two New York, Inc.·G33527000XL1·IIJA COMPLIANT DISPOSABLE ISOLATION GOWN LEVEL ...

    212NY

    FDA UDI
    Two One Two New York, Inc.·00860013168926·LEVEL 2 DISPOSABLE ISOLATION GOWN - 10 PACK

    212NY

    FDA UDI
    Two One Two New York, Inc.·00860013168902·LEVEL 2 DISPOSABLE ISOLATION GOWN-10 PACK

    O-TWO MEDICAL TECHNOLOGIES, INC.

    FDA registration
    O-TWO MEDICAL TECHNOLOGIES, INC.·21 products·🇨🇦 Canada

    MWO-202 3D HYDRAULIC COARSE/FINE MICROMANIPULATOR

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

    SHILEY

    FDA Adverse Event
    Malfunction ·TUBE, BRONCHIAL (W/WO CONNECTOR)·Product code BTS·October 30, 2017

    UNSPECIFIED ENDOTRACH TUBE

    FDA Adverse Event
    Death ·TUBE, TRACHEAL (W/WO CONNECTOR)·Product code BTR·November 11, 2021