BEUDAMED
    27 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 ×

    Optilite High Sensitivity C-Reactive Protein Kit

    FDA 510(k)
    FDA Class 2 ·Immunology

    Nut

    FDA UDI
    I.T.S. GmbH·09120047306857·Nut, Clamp, Quadrilateral Plate

    Cannula, Suction, Needle, Heparin 4.5cm Ø2.0mm

    FDA UDI
    Geister Medizintechnik GmbH·04057034038956·Cannula, Suction, Needle, Heparin 4.5cm ...

    PASS SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ORAL/ENTERAL SYRINGES

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

    PASS LP

    FDA Adverse Event
    Injury ·MEDICREA INTERNATIONAL·Product code MNI·December 23, 2011

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES GRENCHEN·Product code HRS·January 30, 2017

    PASS LP

    FDA Adverse Event
    Injury ·MEDICREA INTL.·Product code MNI·September 16, 2011

    PASS LP

    FDA Adverse Event
    Injury ·MEDICREA INTL.·Product code MNI·October 14, 2011

    PASS LP

    FDA Adverse Event
    Injury ·MEDICREA INTERNATIONAL·Product code MNI·November 11, 2011

    PASS LP

    FDA Adverse Event
    Injury ·MEDICREA INTERNATIONAL·Product code MNI·April 5, 2012

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 27, 2011

    SITTER SELECT

    FDA Adverse Event
    Malfunction ·J. T. POSEY CO.·Product code KMI·June 4, 2013

    ACCU-CHEK ULTRAFLEX INFUSION SET

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS·Product code FPA·September 29, 2008

    PASS LP

    FDA Adverse Event
    Injury ·MEDICREA TECHNOLOGIES·Product code MNI·April 17, 2013

    PASS LP

    FDA Adverse Event
    Injury ·MEDICREA TECHNOLOGIES·Product code MNI·April 17, 2013

    PASS LP

    FDA Adverse Event
    Injury ·MEDICREA·Product code MNI·April 17, 2013

    PULMONETIC

    FDA Adverse Event
    Malfunction ·PULMONETIC SYSTEMS, INC.·Product code CBK·June 20, 2006

    Minimal Access Attachment Product Usage: Pneumatic system

    FDA Enforcement
    Class II ·Terminated·The Anspach Effort, Inc.·May 10, 2017

    Minimal Access Straight Driver Product Usage: Pneumatic system

    FDA Enforcement
    Class II ·Terminated·The Anspach Effort, Inc.·May 10, 2017