Identity
- Trade Name
- Kangaroo FDA UDI
- Generic Name
- Enteral feeding noninvasive-component set FDA UDI
- Device Name
- Epump and Joey Pump Set with Flush Bag Anti-free Flow 500 mL FDA UDI
- Model / Reference
- 674668 FDA UDI
- Description
- Epump and Joey Pump Set with Flush Bag Anti-free Flow 500 mL FDA UDI
Identifiers
- Catalog Number
- 674668 FDA UDI
- Primary DI / UDI-DI
- 10192253008432 FDA UDI
- FDA Product Code
- LZH FDA UDI
- GMDN Term
- Enteral feeding noninvasive-component set FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5725 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 500 Milliliter FDA UDI
Category: Enteral feeding noninvasive-component set
Kangaroo by Cardinal Health 200, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Enteral feeding noninvasive-component set.
- Mini ONE® Balloon Button — Applied Medical Technology, Inc. · Class II
- Mini ONE® Balloon Button — Applied Medical Technology, Inc. · Class II
- Mini ONE® Balloon Button — Applied Medical Technology, Inc. · Class II
- Mini ONE® Balloon Button — Applied Medical Technology, Inc. · Class II
- Mini ONE® Balloon Button — Applied Medical Technology, Inc. · Class II
- Kangaroo — Cardinalhealth · Class II
- Mini ONE® Balloon Button — Applied Medical Technology, Inc. · Class II
- Medline — MEDLINE INDUSTRIES, INC. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Cardinal Health 200, LLC
Sources (1)
- FDA UDI 73c59725-6be6-41ae-af9b-5efa546f7898 35 fields · synced Jun 8, 2026