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

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    XLTEK XCALIBUR EMG / LT, MODEL PK1P33, PK1059

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Harvard Ionoglas Fill Extra A2

    FDA UDI
    Harvard Dental International GmbH·EHAR70521121·Esthetic glass ionomer cement for restorations

    Oph.Forceps

    FDA UDI
    KATENA PRODUCTS, INC.·00841668115978·Tying Forcep, Curved, 3 3/8", Titanium

    RANDOX DIGITOXIN

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    RUBBERCARE POLYMER-CHLORINATED POWDER-FREE GUARDIAN POLYMER-CHLORINATED POWDER-FREE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SLEEPEASY

    FDA Adverse Event
    Injury ·RESPIRONICS INC.·Product code BZD·April 12, 2012

    REMSTAR PLUS M-SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code BZD·May 6, 2010

    REMSTAR M SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code BZD·November 25, 2009

    M-SERIES DC POWER SUPPLY

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·May 25, 2012

    LIFESTENT VALEO BILIARY STENT

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code FGE·December 29, 2009

    M-LNCS DC-I

    FDA Adverse Event
    Malfunction ·MASIMO - 40 PARKER·Product code DQA·November 21, 2016

    M-LNCS DC-I

    FDA Adverse Event
    Malfunction ·MASIMO - 40 PARKER·Product code DQA·November 21, 2016

    LIFESTENT VALEO BILIARY STENT

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code FGE·December 29, 2009

    LIFESTENT VALEO VASCULAR STENT

    FDA Adverse Event
    Injury ·BARD PERIPHERAL VASCULAR, INC.·Product code FGE·August 9, 2010

    LNCS DC-I

    FDA Adverse Event
    Malfunction ·MASIMO - 40 PARKER·Product code DQA·March 11, 2017

    RD SET DCI

    FDA Adverse Event
    Malfunction ·MASIMO - 40 PARKER·Product code DQA·February 17, 2017

    VALEO VASCULAR STENT

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code FGE·September 3, 2010

    QUICK RELEASE T-HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code LXH·April 11, 2013

    EXPRESSEW II NEEDLE

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code HWQ·March 1, 2011

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code FKX·September 2, 2014