BEUDAMED
    12 results · 21ms · 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 ×

    MODELS 6207/6208/6209/6210/6211/6212/6214 (PLI'S)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    3M™ Unitek™

    FDA UDI
    3M COMPANY·30605861028999·3M™ Unitek™ Stainless Steel Permanent First Bic...

    Mobius Elastic Retractor

    FDA UDI
    Coopersurgical, Inc.·00888937003802·Medium; 8-14 cm Incision Range

    Intervertebral Body Fusion Device

    FDA UDI
    PRECISION SPINE, INC.·00840019923262·PLIF Sizer 15mm x 25mm

    PRO OSTEON 200R RESORBABLE BONE GRAFT SUBSTITUTE, MODELS 2RG051, 2RG101, 2RG151, 2RG201, 2RG301, 2RG050, 2RG100, 2RG150,

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ROTAFLOW CENTRIFUGAL PUMP WITH SOFTLINE COATING, MODEL BO-RF-32 (USA)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    1000 ML TPN BAG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code LHI·December 9, 2020

    VENTED MICRO VOL.INLET, N/S

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code LHI·March 28, 2022

    250 ML TPN BAG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code LHI·May 21, 2021

    NAIL,FIXATION,BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JDS·June 27, 2014

    ASR ACETABULAR CUPS 48

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 7, 2013

    RESTORE RECHARGEABLE NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·October 28, 2010