gudid
Primary ID: 674668
Kangaroo (UDI 674668)
Manufactured by Cardinal Health, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kangaroo - Primary ID 674668
Device Regulatory Overview
The Kangaroo (Model/Catalog Number: 674668) is a medical device manufactured by Cardinal Health, Inc.. This product is indexed under FDA Product Code / Category Classification LZH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 674668
- Product Code / EMDN
- LZH
- Device Name
- Epump and Joey Pump Set with Flush Bag,Anti-free Flow
- Database Sync Date
- 2026-08-09 09:42:40
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 Kangaroo?
The registered manufacturer of record for Kangaroo is Cardinal Health, Inc..
What is the Primary UDI-DI identifier for Kangaroo?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 674668.
What classification code is assigned to this device?
This device is registered under product classification code LZH.
Similar Classification Devices (LZH)
Other Devices by Cardinal Health, Inc.
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