gudid
Primary ID: 01-07-1000
FORE-SIGHT (UDI 01-07-1000)
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 - Primary ID 01-07-1000
Device Regulatory Overview
The FORE-SIGHT (Model/Catalog Number: 01-07-1000) 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
- 01-07-1000
- Product Code / EMDN
- MUD
- Device Name
- Tissue Oximeter Sensor (Small Non-adhesive)
- 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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of FORE-SIGHT?
The registered manufacturer of record for FORE-SIGHT is CAS MEDICAL SYSTEMS, INC..
What is the Primary UDI-DI identifier for FORE-SIGHT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 01-07-1000.
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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