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

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    VistaPano S Ceph 2.0 (VistaPano S Ceph); VistaPano S 2.0 (VistaPano S); ProVecta S-Pan Ceph 2.0 (ProVecta S-Pan Ceph); ProVecta S-Pan 2.0 (ProVecta S-Pan)

    FDA 510(k)
    FDA Class 2 ·Dental

    LCP

    FDA UDI
    Synthes GmbH·10886982164513·4.5MM LCP PROXIMAL TIBIA PLATE 8 HOLES/154MM-RIGHT

    N/A

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036035877·

    Spud

    FDA UDI
    KATENA PRODUCTS, INC.·00841668101209·GOLF CLUB FOREIGN BODY SPUD

    SacroFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361023302·Ø8MM FUSION SCREW, GEN II, SACROFUSE, 40MM

    devemed

    FDA UDI
    devemed GmbH·04061644019649·Bone carrier "Ivory" Ø 3.50 / 2.80 mm F-LINE | ...

    Next Generation Sequencing Oncology Panel, Somatic Or Germline Variant Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·Oncomine Dx Express Test

    Universal Base Conical Connection (CC)

    FDA 510(k)
    FDA Class 2 ·Dental

    NIO 5MP MEDICAL GRAYSCALE DISPLAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    Trilogy®

    FDA UDI
    Zimmer, Inc.·00889024119284·

    Next Generation Sequencing Oncology Panel, Somatic Or Germline Variant Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·Oncomine™ Dx Express Test

    Next Generation Sequencing Oncology Panel, Somatic Or Germline Variant Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·Oncomine Dx Express Test

    Next Generation Sequencing Oncology Panel, Somatic Or Germline Variant Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·Oncomine Dx Express Test

    Next Generation Sequencing Oncology Panel, Somatic Or Germline Variant Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·Oncomine Dx Express Test

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 10, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·September 8, 2011

    VERSACARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·July 11, 2013