eudamed_udi
Primary ID: 05060131888507
Rebreath With Valve (UDI 05060131888507)
Manufactured by Reliance Medical Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Rebreath With Valve - Primary ID 05060131888507
Device Regulatory Overview
The Rebreath With Valve (Model/Catalog Number: 850) is a medical device manufactured by Reliance Medical Ltd. This product is indexed under FDA Product Code / Category Classification R9001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 850
- Product Code / EMDN
- R9001
- Device Name
- CPR Face Shields
- Database Sync Date
- 2026-08-09 16:59:51
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 Rebreath With Valve?
The registered manufacturer of record for Rebreath With Valve is Reliance Medical Ltd.
What is the Primary UDI-DI identifier for Rebreath With Valve?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060131888507.
What classification code is assigned to this device?
This device is registered under product classification code R9001.
Similar Classification Devices (R9001)
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