BEUDAMED
    13 results · 21ms · 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 ×

    OneTouch Verio Flex Blood Glucose Monitoring System

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    OT VERIO FLEX METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 1, 2015

    DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169524798·GUIDE 2150214 O51 SCREW GUIDE 14MM

    HHM

    FDA UDI
    Oticon A/S·05707131286390·H160V2 TI, MINIRITE 312 WL SIL HHM

    Accent Buccal Tube

    FDA UDI
    ORMCO CORPORATION·00889989054040·ORTHOS ACCENT LSM 5SGL WDX -10TX18 R

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100073·TEMPORAL SPECULUM SOLID BLADES

    NITRILE POWDER FREE EXAMINATION GLOVES (WHITE)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CORNERSTONE PSR CERVICAL INTERBODY FUSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 4, 2016

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·April 22, 2020

    PAINSMART IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·May 29, 2013

    IN TOUCH ZU

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·June 10, 2011

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM

    FDA Adverse Event
    Injury ·BIOENTERICS, CORP.·Product code LTI·September 3, 2008