BEUDAMED
    12 results · 21ms · Sources: EU EUDAMED, US FDA

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    MAXIM REMOVABLE MOLDED POLY TIBIA

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SW

    FDA UDI
    SW SAFETY SOLUTIONS INC.·00616489997535·PowerForm Nitrile Exam Gloves, Medium

    Medline Sterile Powder-Free Nitrile Examination Gloves - Green (Tested For Use with Chemotherapy Drugs)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ELVIS HSV ID AND D3 TYPING TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    INVISION-PLUS

    FDA Adverse Event
    Malfunction ·RYMED TECHNOLOGIES, LLC·Product code FPA·July 7, 2022

    CVS DISINFECTING LENS CARE SOLUTION

    FDA Adverse Event
    Injury ·KC PHARMACEUTICALS, INC.·Product code LPN·March 6, 2013

    VIRTUOSO DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code LWS·February 15, 2011

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·August 8, 2014

    PLEURX DRAINAGE KIT 500ML 10/CS

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code DWM·July 25, 2025

    PLEURX DRAINAGE KIT 500ML 10/CS

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code DWM·December 24, 2024

    PLEURX DRAINAGE KIT 500ML 10/CS

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code DWM·December 24, 2024

    Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only);

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026