gudid
Primary ID: Genfore
Reliance (UDI Genfore)
Manufactured by Corporation Steris Canada
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Reliance - Primary ID Genfore
Device Regulatory Overview
The Reliance (Model/Catalog Number: Genfore) is a medical device manufactured by Corporation Steris Canada. This product is indexed under FDA Product Code / Category Classification MEC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Genfore
- Product Code / EMDN
- MEC
- Device Name
- Washer Disinfector
- Database Sync Date
- 2026-08-09 09:19:10
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 Reliance?
The registered manufacturer of record for Reliance is Corporation Steris Canada.
What is the Primary UDI-DI identifier for Reliance?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Genfore.
What classification code is assigned to this device?
This device is registered under product classification code MEC.
Similar Classification Devices (MEC)
Other Devices by Corporation Steris Canada
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