gudid
Primary ID: RETBAG01
Reliance (UDI RETBAG01)
Manufactured by STERIS CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Reliance - Primary ID RETBAG01
Device Regulatory Overview
The Reliance (Model/Catalog Number: RETBAG01) is a medical device manufactured by STERIS CORPORATION. This product is indexed under FDA Product Code / Category Classification FMH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RETBAG01
- Product Code / EMDN
- FMH
- Device Name
- Reliance Transport Bags are color coded and tear-resistant bags for clear and immediate identification of clean and dirty scopes.
- 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 STERIS CORPORATION.
What is the Primary UDI-DI identifier for Reliance?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RETBAG01.
What classification code is assigned to this device?
This device is registered under product classification code FMH.
Similar Classification Devices (FMH)
Other Devices by STERIS CORPORATION
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