GUDIDData
gudid Primary ID: 01-06-3014

FORE-SIGHT ELITE (UDI 01-06-3014)

Manufactured by CAS MEDICAL SYSTEMS, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FORE-SIGHT ELITE - Primary ID 01-06-3014

Device Regulatory Overview

The FORE-SIGHT ELITE (Model/Catalog Number: 01-06-3014) is a medical device manufactured by CAS MEDICAL SYSTEMS, INC.. This product is indexed under FDA Product Code / Category Classification MUD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
01-06-3014
Product Code / EMDN
MUD
Device Name
Tissue Oximeter Battery Pack
Database Sync Date
2026-08-09 09:31:01

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of FORE-SIGHT ELITE?

The registered manufacturer of record for FORE-SIGHT ELITE is CAS MEDICAL SYSTEMS, INC..

What is the Primary UDI-DI identifier for FORE-SIGHT ELITE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 01-06-3014.

What classification code is assigned to this device?

This device is registered under product classification code MUD.

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