gudid
Primary ID: Single Chamber
Vision (UDI Single Chamber)
Manufactured by Corporation Steris Canada
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vision - Primary ID Single Chamber
Device Regulatory Overview
The Vision (Model/Catalog Number: Single 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
- Single Chamber
- Product Code / EMDN
- MEC
- Device Name
- The Vision Single-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), theater shoes and other similar and related items found in healthcare facilities.
- Database Sync Date
- 2026-08-09 09:19:10
Full Regulatory Attributes
🔒 Token Gated
{
"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 Vision?
The registered manufacturer of record for Vision is Corporation Steris Canada.
What is the Primary UDI-DI identifier for Vision?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Single 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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