gudid
Primary ID: FD81000
NA (UDI FD81000)
Manufactured by Corporation Steris Canada
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID FD81000
Device Regulatory Overview
The NA (Model/Catalog Number: FD81000) 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
- FD81000
- Product Code / EMDN
- MEC
- Device Name
- The Two Level Manifold Rack with Equal Level Space, Large is used to hold loaded instrument trays during processing in the 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 NA?
The registered manufacturer of record for NA is Corporation Steris Canada.
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FD81000.
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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