BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    NANCY NAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295233503·P.F.C. SIGMA TIBIAL COMPONENT ALL POLY CURVED 3...

    DUTECK BODY COMPOSITION ANALYZER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Medline ENFit Syringe

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

    GYNECARE MESH UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·August 3, 2015

    3.7MM TI CERV SPN SCR SLF-DRLGVARIABLE ANGLE 16MM-STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES·Product code ODP·February 14, 2013

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·July 21, 2014

    Depuy P.F.C. E knee system, all polyethylene curved tibial component, Sz 3, 12.5 mm; Ref 96-0642.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·May 26, 2005

    Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026