BEUDAMED
    55 results · 25ms · 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 ×

    STRATAFIX Symmetric PDS Plus Knotless Tissue Control Devices, STRATAFIX Spiral PDS Plus Knotless Tissue Control Devices, STRATAFIX Spiral MONOCRYL Plus Knotless Tissue Control Devices, STRATAFIX Spiral MONOCRYL Knotless Tissue Control Devices

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

    SFXSPI PDS+ UNI VIO 6IN 3-0 SA SH

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code NEW·October 24, 2024

    Bernafon

    FDA UDI
    Bernafon AG·05711584081600·ZERENA 5 B 105 FW 1.0

    MEDTRONIC ANGIOGRAPHIC GUIDE WIRES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VASOPOUSE DEEP VEIN THROMBOSIS COMPRESSION DEVICE MODEL IPCS, MODEL SQS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MUSTMINI OCCIPITAL SCREW

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·February 11, 2025

    2600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 11, 2011

    UNKNOWN DEPUY MENISCAL BEARINGS

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code JWH·June 21, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 17, 2014

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·April 2, 2021

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 9, 2019

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 11, 2024

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·February 20, 2020

    SENRI

    FDA Adverse Event
    Injury ·KANEKA·Product code LIT·March 12, 2019

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·May 6, 2025

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·December 24, 2025

    DIVA

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

    DIVA

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 12, 2020

    18 SHIDEN HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 19, 2025