gudid
Primary ID: 22855
Kendall (UDI 22855)
Manufactured by Cardinal Health, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kendall - Primary ID 22855
Device Regulatory Overview
The Kendall (Model/Catalog Number: 22855) is a medical device manufactured by Cardinal Health, Inc.. This product is indexed under FDA Product Code / Category Classification DRX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 22855
- Product Code / EMDN
- DRX
- Device Name
- 855 Foam Electrodes,Conductive Adhesive Hydrogel, Radiolucent
- Database Sync Date
- 2026-08-09 09:00:28
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 Kendall?
The registered manufacturer of record for Kendall is Cardinal Health, Inc..
What is the Primary UDI-DI identifier for Kendall?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 22855.
What classification code is assigned to this device?
This device is registered under product classification code DRX.
Similar Classification Devices (DRX)
Other Devices by Cardinal Health, Inc.
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