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

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    SAS ADENO TEST

    FDA 510(k)
    FDA Class 1 ·Microbiology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517404282·CoRoent® XLT, 6x16x30mm

    NOBEL BIOCARE ENDOSSEOUS IMPLANTS (MAXILLOFACIAL INDICATION)

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

    SolidAIRity III Airway Stabilization System

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 8, 2006

    CONSERVE(R) PLUS HA CUP

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·March 5, 2013

    BIOPLATE TITANIUM FIXATION SYSTEM

    FDA Adverse Event
    Injury ·BIOPLATE·Product code JEY·February 11, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014

    UNKNOWN

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·June 9, 2021

    ZIMMON PANCREATIC STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·October 16, 2020

    BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER

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