gudid
Primary ID: Multi-Chamber
Reliance Vision (UDI Multi-Chamber)
Manufactured by Corporation Steris Canada
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Reliance Vision - Primary ID Multi-Chamber
Device Regulatory Overview
The Reliance Vision (Model/Catalog Number: Multi-Chamber) 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
- Multi-Chamber
- Product Code / EMDN
- MEC
- Device Name
- The Reliance Vision Multi-Chamber Washer Disinfector is intended for use in the cleaning and intermediate level disinfection of soiled reusable utensils, trays, glassware, bedpans and urinals, rubber and plastic goods, simple hard-surfaced rigid surgical instruments (such as forceps and clamps) and other related articles found in healthcare facilities.
- Database Sync Date
- 2026-08-09 09:19:09
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 Vision?
The registered manufacturer of record for Reliance Vision is Corporation Steris Canada.
What is the Primary UDI-DI identifier for Reliance Vision?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Multi-Chamber.
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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