BEUDAMED
    63 results · 66ms · Sources: EU EUDAMED, US FDA

    MEDICAL BIOPSY AUTOMATIC CUTTING NEEDLE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SURGICAL STAPLE MARKER DEVICE (MODIFY)

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

    BIOPSY DEVICE ACCESSORY

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

    BIOPSY NEEDLE AND HOUSING

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    RETRACTOR ARM CLAMP

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    BIOPSY NEEDLE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    MAMMOTOME BIOPSY PROBE AND HOUSING (MAMMOTOME)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    FORCEPS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    BIOPSY DEVICE ACCESSORY

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    NEEDLE GUIDE

    FDA 510(k)
    FDA Class 2 ·Radiology

    BIOPSY NEEDLE AND HOUSING

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    MODIFIED BIOPSY NEEDLE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Multi-Analyte Test System With Algorithmic Analysis For Detection Of Prostate Cancer

    FDA Pre-Market Approval
    FDA Class 3 ·4Kscore Test

    Insight Instruments, Inc. Vitreous Biopsy Probe 27 Ga

    FDA UDI
    INSIGHT INSTRUMENTS, INC.·00852475007011·Dispenser Box of 5 Each Sterile Disposable 27 G...

    Insight Instruments, Inc. Vitreous Biopsy Probe 27 Ga

    FDA UDI
    INSIGHT INSTRUMENTS, INC.·00852475007004·1 Each Sterile Disposable 27 Ga Vitreous Biopsy...

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

    FDA Pre-Market Approval
    FDA Class 3 ·Guardant360 CDx

    Forceps, Biopsy, Electric, Reprocessed

    FDA classification
    FDA Class 2 ·Forceps, Biopsy, Electric, Reprocessed

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

    FDA Pre-Market Approval
    FDA Class 3 ·RESOLUTION ctDx FIRST

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

    FDA Pre-Market Approval
    FDA Class 3 ·FoundationOne Liquid CDx (F1 Liquid CDx)

    Cervical Intraepithelial Neoplasia (Cin) Test System

    FDA classification
    FDA Class 2 ·Cervical Intraepithelial Neoplasia (Cin) Test System