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

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    Navigation Module of the Momentum System

    FDA 510(k)
    FDA Class 2 ·Neurology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772777624·LUMBAMED BASIC DORSAL STAYS WM SILVER V

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517295828·CoRoent® XL-H, 8x22x45mm 20°

    CASTANARES SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896055858·CASTANARES SCISSORS STRAIGHT BLADES POWER CUT B...

    Ophthalmic Spatulas

    FDA UDI
    KATENA PRODUCTS, INC.·00841668114322·RUBENSTEIN CORNEAL ROLLER (BX/3)

    Vu aPod™ - L

    FDA UDI
    Seaspine Orthopedics Corporation·10889981046132·LATERAL IMPLANT, WIDE, STANDARD, 8mm X 23mm X 45mm

    EMIT 2000 VANCOMYCIN CALIBRATORS

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    MODIFICATION TO JMS A.V. FISTULA NEEDLE SET

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

    TRUFIT CB PLUG, PURPLE 11MM

    FDA Adverse Event
    Malfunction ·MANSFIELD·Product code MQV·November 12, 2009

    TRUFIT CB PLUG PURPLE, 11MM

    FDA Adverse Event
    Malfunction ·MANSFIELD·Product code MQV·November 12, 2009

    BD INSULIN SYRINGE WITH BD ULTRA-FINE¿ NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·March 4, 2022

    ICY HOT MEDICATED PATCH EXTRA STRENGTH

    FDA Adverse Event
    Injury ·CHATTEM·Product code IMD·May 17, 2008

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 20, 2008

    INTERSTIM II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·August 8, 2011

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 2, 2013

    PLATE,FIXATION,BONE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·January 24, 2019

    PLATE,FIXATION,BONE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·January 24, 2019

    PLATE,FIXATION,BONE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·January 24, 2019

    PLATE,FIXATION,BONE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·January 24, 2019

    Cannula and Seal; 5mm x 100mm and 12mm x 100mm Model #: CTS02 and CTS22. Indicated for use to establish a port of entry fro endoscopic instruments in patients requiring minimally invasive surgical procedures including thoracic, gynecologic laparoscopy and other abdominal procedures.

    FDA Enforcement
    Class II ·Terminated·Stryker Sustainability Solutions·July 1, 2015