BEUDAMED
    28 results · 24ms · 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 ×

    Sof-Flex Ureteral Stent Set

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SOF-FLEX MULTI-LENGTH URETERAL STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·October 24, 2024

    SOF-FLEX PEDIATRIC DOUBLE PIGTAIL URETERAL STENT SET

    FDA Adverse Event
    Injury ·COOK INC·Product code FAD·September 30, 2024

    SOF-FLEX PEDIATRIC DOUBLE PIGTAIL URETERAL STENT SET

    FDA Adverse Event
    Injury ·COOK INC·Product code FAD·October 7, 2024

    SOF-FLEX MULTI-LENGTH URETERAL STENT SET

    FDA Adverse Event
    Injury ·COOK INC·Product code FAD·October 21, 2024

    SOF-FLEX PEDIATRIC DOUBLE PIGTAIL URETERAL STENT SET

    FDA Adverse Event
    Injury ·COOK INC·Product code FAD·April 19, 2021

    SOF-FLEX PEDIATRIC DOUBLE PIGTAIL URETERAL STENT SET

    FDA Adverse Event
    Injury ·COOK INC·Product code FAD·April 19, 2021

    SOF-FLEX PEDIATRIC DOUBLE PIGTAIL URETERAL STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·June 28, 2022

    SOF-FLEX MULTI-LENGTH URETERAL STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·October 21, 2024

    ProFil

    FDA UDI
    SILMET LTD·07290015358545·Dental Composite Restorative

    PFT Kit C

    FDA UDI
    A-M SYSTEMS, LLC·00817081021240·PFT Kit C, 35mm Kit - Case

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694004947·125mm x 180mm Mesh Plate, Rigid, 1.6mm

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K1100530·Caddie, 7.5mm Screws

    MATTIOLI PULSE TWO/THREE PLUS FAMILY

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

    CORRECTINJECT SAFETY SYSTEM, CATHETER CONNECTOR, FILTER, INFUSION ADAPTOR, SYRINGE KIT

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    AMISTEM-H PROXIMAL COATING STD STEM SIZE 2

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·October 19, 2018

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 27, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 20, 2013

    PUMP MMT-722RNAS PRDGM INS SK EN RC

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code LZG·September 26, 2008

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·July 3, 2018