Home GUDID 00860015781925 Bunkerhill Contrast AVC
Primary DI 00860015781925
Brand Bunkerhill Contrast AVC
Company Bunkerhill Health Inc.
Model 1.0.0
Device description Bunkerhill Contrast AVC is a software device intended for use in detecting presence and estimating quantity of aortic valve calcification for adult patients aged 40 years and above
Published 2026-09-16
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile false
Single use true Product Codes# Code, Name table Code Name JAK System, X-Ray, Tomography, Computed
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class JAK System, X-Ray, Tomography, Computed Radiology 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00860015781925 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00860015781925 00860015781925 860015781925 0860015781925
GMDN Terms# Term, Definition table Term Definition Chest/vascular CT/MRI clinical assessment support software A software program intended to display, analyse/process, and possibly acquire computed tomography (CT) and/or magnetic resonance imaging (MRI) data of the chest anatomy (e.g., lungs, heart) and/or vascular system, to support a healthcare provider with clinical assessment (e.g., diagnosis, triage) of a pulmonary, cardiac and/or vascular condition (e.g., pulmonary embolism, coronary artery disease, abdominal aortic aneurysm, cancer). It is not dedicated to treatment planning, neurovascular or orthopaedic image analysis, and does not incorporate adaptive/dynamic machine learning (ML) models.
Regulatory Flags# DUNS number 117220923 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch false Serial number false Manufacturing date on label false Expiration date on label false Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00860015781918 iCAC Device 1.0.0 2026-05-31 00860015781901 CAC (Gated) Algorithm 1 2026-05-13
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