gudid
Primary ID: FD80200
N/A (UDI FD80200)
Manufactured by Corporation Steris Canada
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for N/A - Primary ID FD80200
Device Regulatory Overview
The N/A (Model/Catalog Number: FD80200) 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
- FD80200
- Product Code / EMDN
- MEC
- Device Name
- The Upper universal insert used with 7052HP and 7053HP Washer Disinfectors.
- 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 N/A?
The registered manufacturer of record for N/A is Corporation Steris Canada.
What is the Primary UDI-DI identifier for N/A?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FD80200.
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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