gudid Primary ID: 01-07-1103

FORE-SIGHT ELITE (UDI 01-07-1103)

Manufactured by CAS MEDICAL SYSTEMS, INC.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The FORE-SIGHT ELITE (Model/Catalog Number: 01-07-1103) 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: 01-07-1103
Product Code / EMDN: MUD
Device Name: Tissue Oximeter Sensor (Large)
Database Sync Date: 2026-08-09 09:31:01

Full Regulatory Attributes

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{
    "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 01-07-1103.

What classification code is assigned to this device?

This device is registered under product classification code MUD.

Similar Classification Devices (MUD)

Other Devices by CAS MEDICAL SYSTEMS, INC.

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