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

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    ACU-GUARD

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    PAQ.150X100X150*N3*HP.M1911A.

    FDA UDI
    AB MEDICA GROUP, S.A.·08428763009153·

    WATER TRAP, SELF SEALING, RIGHT ANGLED, HIGH VOLUME

    FDA UDI
    Intersurgical Incorporated·05030267056217·WATER TRAP, SELF SEALING, RIGHT ANGLED, HIGH VO...

    nSpire Health

    FDA UDI
    NSPIRE HEALTH, INC.·10852417003597·KoKo Elliptical Pulmonary Function Filter, Whit...

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·04546540393807·UNIVERSAL NEURO MODULE

    Mustang Knotless Suture Anchor

    FDA UDI
    RESPONSIVE ORTHOPEDICS LLC·00811714035574·Mustang Knotless Suture Anchor, 4.75mm

    Mustang Knotless Suture Anchor

    FDA UDI
    RESPONSIVE ORTHOPEDICS LLC·00811714035581·Mustang Knotless Suture Anchor, 5.5mm

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0150000·Driver Shaft, T15, Cross Link Final Driver

    MATIRA ANTERIOR CERVICAL SYSTEM

    FDA UDI
    Kalitec Direct LLC·B07307K0150001·GUIDE, AIO FIXED SINGLE

    HOWMEDICA KINEMAX PLUS TOTAL KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ALOKA UST-964P-5 ENDOVAGINAL TRANSDUCER

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

    METHADONE METABOLITE (EDDP) ENZIME IMMUNOASSAY, CAT. NO. 190 (500 TEST KIT), NO. 191 (5000 TEST KIT)

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·January 15, 2013

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·November 17, 2010

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 6, 2014