gudid
Primary ID: FGR10500 0000
Carex (UDI FGR10500 0000)
Manufactured by Drive Devilbiss Healthcare
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Carex - Primary ID FGR10500 0000
Device Regulatory Overview
The Carex (Model/Catalog Number: FGR10500 0000) is a medical device manufactured by Drive Devilbiss Healthcare. This product is indexed under FDA Product Code / Category Classification BYX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FGR10500 0000
- Product Code / EMDN
- BYX
- Device Name
- Oxygen Tubing 25'with green tint
- Database Sync Date
- 2026-08-09 09:00:33
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 Carex?
The registered manufacturer of record for Carex is Drive Devilbiss Healthcare.
What is the Primary UDI-DI identifier for Carex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FGR10500 0000.
What classification code is assigned to this device?
This device is registered under product classification code BYX.
Similar Classification Devices (BYX)
Other Devices by Drive Devilbiss Healthcare
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