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

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    SHENLING ACUPUNCTURE NEEDLES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BetaForce

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730022349·Beta3 Lengths 19x25 10 per pack, 14" lengths

    BetaForce™

    FDA UDI
    Ortho Organizers, Inc.·00190707124717·BETAFORCE Beta³ Lengths 19x25 (10pk), 14" lengths

    RR - UP - Commuter Passenger - zlb

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588024110·RR - UP - Commuter Passenger - zlb

    Battalion

    FDA UDI
    ALPHATEC SPINE, INC.·00840967188874·Battalion, LLIF Trial, 0°, 24 mm Wide, 11 mm X ...

    XIPHOS ZFUZE

    FDA UDI
    Difusion Technologies, Inc.·00853896008243·TLIF Spacer 24mm Long x 11mm Height

    CHILI VIDEO, CHILI VIDEOPRO

    FDA 510(k)
    FDA Class 2 ·Radiology

    WHOLE PTH (1-84) SPECIFIC IMMUNORADIOMETRIC IRMA DIAGNOSTIC ASSAY KIT, MODEL 3KG056

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    COMPR SRS 50MM DST HUM BDY RT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·May 31, 2019

    NA

    FDA Adverse Event
    Malfunction ·STERILMED, INC.·Product code NLM·March 8, 2013

    PRIMA ESTH CON ZI ABUT WD 6.0X1.5MM

    FDA Adverse Event
    Malfunction ·KEYSTONE DENTAL·Product code NHA·January 28, 2011

    ENDOTAK RELIANCE G

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC·Product code LWS·February 7, 2008

    TEMPOROMANDIBULAR JOINT SMALL LEFT FOSSA COMPONENT

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·May 24, 2016

    CROSS-DRIVE EMERGENCY SCREW 3.2 X 10 MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·May 24, 2016

    2.7 X 10 MM HIGH TORQUE CROSS-DRIVE SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·May 24, 2016

    2.0 X 11 MM FOSSA CROSS-DRIVE SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·May 24, 2016

    45MM LEFT STANDARD MANDIDUBLAR COMPONENT TMJ

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·May 24, 2016

    COCR FEMORAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code JDI·May 14, 2018

    CER OPTION TYPE 1 TPR SLEVE -3

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code OQG·June 8, 2021

    45MM LEFT STANDARD MANDIBLE

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·May 24, 2016