BEUDAMED
    22 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 ×

    OBS Anchorage Screw, Biokey Anchorage Screw

    FDA 510(k)
    FDA Class 2 ·Dental

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112991·CORNEAL TREPHINE BLADE16MM

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112632·BARRON CORNEAL PUNCH 8.0MM

    Navajo Tribal Utility Authority - 18 Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588012780·Navajo Tribal Utility Authority - 18 Metal

    BROOKER FEMORAL NAILS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TMD SAFETY SYRINGE (FA12 SERIES 3ML/FA13 SERIES 5ML)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VALIANT STENT GRAFT

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code MIH·January 25, 2022

    TALENT - UNK

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code MIH·January 25, 2022

    TALENT - UNK

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·January 25, 2022

    VALIANT STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·January 25, 2022

    ENDURANT STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·January 11, 2022

    ENDURANT STENT GRAFT

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code MIH·January 11, 2022

    ENDURANT II STENT GRAFT

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code MIH·January 19, 2022

    UNKNOWN DEPUY PATELLA

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code JWH·October 27, 2014

    ENRHYTHM DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DXY·August 11, 2011

    ACUVUE OASYS

    FDA Adverse Event
    Malfunction ·JOHNSON AND JOHNSON VISION CARE·Product code LPL·June 26, 2013

    ANGIOJET SOLENT OMNI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KRA·June 17, 2022

    MONOCRYL POLIGLECAPRONE 25 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAN·May 4, 2022

    MANTA 14F

    FDA Adverse Event
    Malfunction ·ESSENTIAL MEDICAL, INC·Product code MGB·September 15, 2022

    PUMP MMT-1780KPK 670G PATHWAY BLACK MG

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·November 17, 2023