BEUDAMED
    2,941 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.
    Filters Regulation: Us FDA ×

    TOWEL OR 17X24IN BLUE STERILE 4/PK

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH SHANGHAI·Product code FRL·February 5, 2020

    KARL STORZ ALLIGATOR FORCEPS

    FDA Adverse Event
    Other ·KARL STORZ GMBH & CO.·Product code JEK·March 21, 1994

    RIGID 3 PRONG GRASPER FOR RETRIEVAL OF STONES

    FDA Adverse Event
    Malfunction ·GYRUS ACMI INC·Product code JEK·January 24, 2014

    MICROVASIVE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code JEK·January 7, 1992

    RIGID GRASPING FORCEPS

    FDA Adverse Event
    Malfunction ·R. WOLF, GMBH·Product code JEK·July 18, 1994

    JACKSON ANG 6MM CUP FCPS 28CM

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code JEK·October 6, 2022

    PILLING

    FDA Adverse Event
    Malfunction ·TELEFLEX INCORPORATED·Product code JEK·September 20, 2022

    RIGID 3-PRONG GRASPER FOR RETRIEVAL OF STONES

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC.·Product code JEK·July 29, 2010

    ESI STANDAD BRONCHOSCOPE FORCEP

    FDA Adverse Event
    Injury ·ENDO-SCIENTIFIC·Product code JEK·February 1, 1993

    Forceps, Biopsy, Bronchoscope (Rigid)

    FDA classification
    FDA Class 2 ·Forceps, Biopsy, Bronchoscope (Rigid)

    JEB TECHNOLOGIES LIMITED

    FDA registration
    JEB TECHNOLOGIES LIMITED·3 products·🇬🇧 United Kingdom

    JAK DIVERSIFIED II, INC.

    FDA registration
    JAK DIVERSIFIED II, INC.·3 products·🇺🇸 United States

    CARCINO-CEK

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    DONG GUAN EEK ELECTRONIC TECHNOLOGY CO.,LIMITED

    FDA registration
    DONG GUAN EEK ELECTRONIC TECHNOLOGY CO.,LIMITED·2 products·🇨🇳 China

    ORTHO-J, INC. BEK-JS-004

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    PATIENT EXAM GLOVES (MFG. AEK RUBBER PRODUCTS)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ITL Dental

    FDA UDI
    EMERY ENTERPRISES INC·00817686024417·BEK Bone Expander Kit

    Compliance EndoKit™

    FDA UDI
    BOSTON SCIENTIFIC CORPORATION·00191506047511·

    Compliance EndoKit™

    FDA UDI
    BOSTON SCIENTIFIC CORPORATION·00840253117946·Compliance EndoKit

    Compliance EndoKit™

    FDA UDI
    BOSTON SCIENTIFIC CORPORATION·00191506010164·Compliance EndoKit