BEUDAMED
    28 results · 23ms · Sources: EU EUDAMED, US FDA

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    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NexTemp

    FDA UDI
    PREMIER DENTAL PRODUCTS COMPANY·00348783000207·NexTemp Bulk Pack Opaque

    Custom Procedure Kit

    FDA UDI
    MEDIVATORS INC.·40677964012868·The ENDO CARRY-ON Procedure Kit contains all of...

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·10304040054625·Polycarbonate Crowns

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001470·artVeneer life upper anteriors, BOM, D3

    DERMAHOOK 1/2 HOOK 10 PKG/BX 6 HKS/PKG

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code HAO·May 6, 2019

    DERMAHOOK 1/2 HOOK 10 PKG/BX 6 HKS/PKG

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code HAO·May 6, 2019

    DERMAHOOK 1/2 HOOK 10 PKG/BX 6 HKS/PKG

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code HAO·May 6, 2019

    DURAHOOK 1/4 HOOK 10 PKG/BX 6 HKS/PKG

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GDG·April 3, 2018

    DURAHOOK 1/4 HOOK 10 PKG/BX 6 HKS/PKG

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GDG·April 3, 2018

    CRONUS GUIDEWIRE, MODEL 001-001470-1

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DERMAHOOK 1/2 HOOK 10 PKG/BX 6 HKS/PKG

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code HAO·April 27, 2017

    SKIN AND SCALP CLIPS AND RETRACTORS

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GAG·May 9, 2018

    DURAHOOK 1/4 HOOK 10 PKG/BX 6 HKS/PKG

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GDG·April 3, 2018

    DERMAHOOK 1/2 HOOK 10 PKG/BX 6 HKS/PKG

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code HAO·May 1, 2017

    RADIOMED SOURCE

    FDA 510(k)
    FDA Class 2 ·Radiology

    GYRUS ENDOUROLOGY SYSTEM: AXIPOLAR RESECTOSCOPE LOOP ELECTRODE

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

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 5, 2013

    CATH INF .038 F4 100 JR-4

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code DQO·February 25, 2011

    10X30 CALAXO SCREW

    FDA Adverse Event
    Other ·SMITH & NEPHEW INC., ENDOSCOPY DIVISON·Product code HWC·February 19, 2008