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

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    SUTURTEK FASTCLOSE FASCIA CLOSURE DEVICE

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

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·H65810111050·DNT BASE REPR LT FIBER SC (5 LBS 4 PER CASE)

    IMPACT-PLUS

    FDA UDI
    Denplus Inc·D8451011105·IMPACT-PLUS, LPI, 454 g

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040013724·Zirlux 16+ D3 98.5X16

    2011 105

    Device
    EU MDR · Eu Md Class 1 ·VOE , S.A·On the market

    5011 105

    Device
    EU MDR · Eu Md Class 1 ·VOE , S.A·On the market

    3011 105

    Device
    EU MDR · Eu Md Class 1 ·VOE , S.A·On the market

    Alleset

    FDA UDI
    GRI Medical & Electronic Technology Co., Ltd.·16931918147291·Leggings Drape_31inx54in_Non-sterile_72EA/CS

    Zavation

    FDA UDI
    Zavation LLC·00197157009847·10.5mm TAP, CANNULATED

    6.5 Cancellous Bone Shaft Screw, hex, St.Steel, L 105/32 mm

    FDA UDI
    mahe medical gmbh·EMAH00100111050·6.5 Cancellous Bone Shaft Screw, hex, St.Ste...

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659173910·6.5 Cancellous Bone Shaft Screw, hex, _x000D_...

    Alleset

    FDA UDI
    GRI Medical & Electronic Technology Co., Ltd.·16931918178608·Leggings Drape_31inx54in_Sterile_50ea/cs

    MOSS MIAMI 6.35MM ROD SYSTEM PEDICLE AND LAMINAR HOOKS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PURE WATER SOLUTIONS CENTRAL WATER SYSTEM FOR HEMODIALYSIS

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

    BD PLASTIPAK¿ SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·October 29, 2021

    PROLITE MESH

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORP.·Product code FTL·March 13, 2013

    FREESTYLE LITE

    FDA Adverse Event
    Malfunction ·Product code NBW·March 8, 2011

    TENDRIL SDX

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2008

    BD INTREGRA¿ SYRINGE WITH DETACHABLE NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code MEG·September 3, 2021

    Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, K011905, Catalog Number: 00-AG387307, .035/150cm, stiff/straight/standard, sold as a single hydrophilic guidewire in both sterile and bulk non-sterile packaging configurations. Argon Medical Devices, Inc. Athens, TX 75751

    FDA Recall
    Terminated ·Argon Medical Devices, Inc·Product code DQX·November 19, 2007