BEUDAMED
    24 results · 28ms · 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 ×

    REDAPT Porous Acetabular Shell

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    K181166

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·December 2, 2022

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·July 15, 2020

    I-LIPO, MODELS A00-1238 (230V), A00-1239 (120V)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    KUMAR T-ANCHORS HERNIA SET

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·August 17, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·May 21, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·August 12, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·July 8, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·July 8, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·June 26, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·July 8, 2020

    TRILOGY EVO, O2, BRAZIL

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·September 6, 2024

    TRILOGY EVO, BRAZIL

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·September 6, 2024

    STIMQ PERIPHERAL NERVE STIMULATOR (PNS) SYSTEM

    FDA Adverse Event
    Injury ·STIMWAVE TECHNOLOGIES INC.·Product code GZF·December 20, 2018

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·August 19, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·July 24, 2020

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·July 7, 2020

    S-ROM M HEAD 36MM +3

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·June 21, 2013

    TRIAL 60-CM LENGTH PERCUTANEOUS LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 21, 2011