BEUDAMED
    28 results · 22ms · Sources: EU EUDAMED, US FDA

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    COMPASS GLOBAL PRESSURE, COMPASS THORACENTESIS, PARACENTESIS, COMPARTMENT PRESSURE, EPIDURAL ASSIST, ARTERIAL ASSIST

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814664·GENUMEDI SILVER SIZE III

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772813834·GENUMEDI PRO SILVER SIZE III

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526749788·MANUMED RFX FRACTURE BRACE, LEFT SIZE 3

    simex

    FDA UDI
    SIMEX Medizintechnik GmbH·04052262413513·Suction tube, sterile, CH21, 180cm with clamp, ...

    IMPACT LIP-LOC HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304211803·

    DD tempMED

    FDA UDI
    Dental Direkt GmbH·EDDIK112201·DD tempMED are pre-colored dental milling blank...

    Pro-Link Stand-Alone Cervical Spacer System

    FDA UDI
    Life Spine, Inc.·00190837059934·

    T-Crystal cartridges Standard Pink

    FDA UDI
    PERFLEX LTD·07290110506339·5 identical cartridges sealed in a vacuum bag ;...

    CHEMTRUE SINGLE / MULTI DRUG SCREEN CASSETTE / DIP CARD TESTS

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    CLAY-PARK LABS, INC. - LUBRICATING JELLY

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    K2M General Instruments

    FDA UDI
    VB Spine LLC·10888857529878·Replaceable Tip

    CM TITAMAX EX IMPLANT 4.0X11

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·November 9, 2017

    CASPIAN Spinal System

    FDA UDI
    VB Spine LLC·10888857216655·Vise Grips Size Ø3.5 mm

    OFFSET 30 DEGREES BROACH HANDLE - LEFT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code GET·July 10, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 14, 2013

    CALIBRATED DRILL BIT 3.1MM X 285MM, AO

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS SELZACH·Product code LXH·April 29, 2011

    DCA 2000 SYSTEM FOR HBA1C

    FDA Adverse Event
    Other ·BAYER CORP.·Product code LCP·August 6, 2008

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·January 20, 2022

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·February 4, 2022