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

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    THE PROMA PERCEPTION, RESPONSE AND COMPASS SYSTEM AND ACCESSORIES

    FDA 510(k)
    FDA Class 1 ·Dental

    Pacific Blue™ anti-human CD16

    FDA UDI
    BIOLEGEND, INC.·00810034700414·URL: https://www.biolegend.com/en-us/products/p...

    DeltaForm HD

    FDA UDI
    Merz Dental GmbH·D7091980106·DeltaForm HD upper posteriors, S, C2 -MADE IN G...

    Handle

    FDA UDI
    Spierings Orthopaedics B.V.·08720254007847·

    SKINTACT PRE-WIRED ECG ELECTRODES WITH CONDUCTIVE ADHESIVE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ThinkQA

    FDA 510(k)
    FDA Class 2 ·Radiology

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 5, 2014

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·February 27, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 24, 2011

    REVISION MODULAR NECK H.60MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code LZO·January 17, 2024

    Angiotech Pediatric Bone Marrow Needle. Pediatric Bone Marrow Needle. STERILE. Product Number: ION18015. 510k K980196. MEDICAL DEVICE TECHNOLOGIES, INC. 3600 Southwest 74th Avenue, Gainesville, Florida 32608 U.S.A. Intended Use: Pediatric Bone Marrow Needle

    FDA Recall
    Terminated ·Medical Device Technologies, Inc.·Product code KNW·September 1, 2009