BEUDAMED
    37 results · 24ms · Sources: EU EUDAMED, US FDA

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    Latex Powder Free Surgical Glove with Protein Labelling Claim of 50 Microgram or Less per Gram of Glove and Tested for use with Chemotherapy Drugs

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    DJO SURGICAL

    FDA UDI
    Encore Medical, L.P.·00190446872016·SPECIAL, EMPOWR REVISION KNEE KEEL TRIAL TOP IN...

    HHM

    FDA UDI
    Oticon A/S·05707131351500·G500 SC, BTE PP 13 2.4G 105 C044 TAR HHM

    MSI

    FDA UDI
    Modern Surgical Instruments LLC·00810130202041·8" Vein Retractor, with Loop Handle

    MSI

    FDA UDI
    Modern Surgical Instruments LLC·B4192017480·

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776191986·VEIN RETRACTOR BLADE LENGTH

    Symmetry Surgical

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482057711·Symmetry® Retractor, Custom Vein, 8 in

    MEDIS 5MP2 QUAD-HEAD MEDICAL DIAGNOSTIC DISPLAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    ENDIUS ATAVI SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·June 12, 2019

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·June 12, 2019

    PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code NEW·July 23, 2018

    UNKNOWN

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code LWR·October 14, 2008

    ATTAIN OTW

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2011

    LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (LARGE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·June 28, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 26, 2013

    HAKIM PROGRAMMABLE VALVE

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES SWITZERLAND SAR·Product code JXG·August 28, 2020

    2182208-2017-00695

    FDA Adverse Event
    Injury ·Product code GEH·May 12, 2017

    UNKNOWN EGIA TRI STAPLE

    FDA Adverse Event
    Injury ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·June 14, 2021

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·June 12, 2019