BEUDAMED
    32 results · 22ms · 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 ×

    VENTRALIGHT (TM) ST MESH WITH ECHO PS (TM) POSITIONING SYSTEM

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

    DD tempMED

    FDA UDI
    Dental Direkt GmbH·EDDIK110201·DD tempMED are pre-colored dental milling blank...

    Valencia Skin Applicator

    FDA UDI
    Nucletron B.V.·08717213036413·Valencia Ft Skin Applicator Set

    VascuTape Radiopaque Tape

    FDA UDI
    Lemaitre Vascular, Inc.·00840663100385·Glow 'N Tell 55cm Tape (20 Strips)

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306818677·Malleable Retractor 3" x 12" w/Protective Edge

    neoWave LS

    FDA UDI
    XENIX MEDICAL LLC·00818345023871·BAYONETTED STRAIGHT RING CURETTE

    NON-STERILE, BLUE & WHITE POWDERED NITRILE EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    WENZEL SPINE VARILIFT INTERBODY FUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DONJOY

    FDA UDI
    DJO, LLC·00888912152631·DRESSING, RECTANGLE,XL,STERILE

    LANCETS

    FDA Adverse Event
    Malfunction ·BD·Product code FMK·April 6, 2012

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·February 6, 2014

    PRISMAFLEX

    FDA Adverse Event
    Death ·GAMBRO LUNDIA AB·Product code KDI·April 11, 2014

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·November 2, 2012

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·February 15, 2012

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·December 23, 2013

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 9, 2013

    RATCHETING SMALL STRAIGHT HANDLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code OLO·September 23, 2014

    UNICEL® DXC 880I SYNCHRON® ACCESS® CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·June 1, 2011

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·February 6, 2014

    PRISMAFLEX

    FDA Adverse Event
    Death ·GAMBRO LUNDIA AB·Product code KDI·January 10, 2014