Identity
- Trade Name
- Kangaroo FDA UDI
- Generic Name
- Enteral tube extension, single-use FDA UDI
- Device Name
- MICROBORE EXT SET BIFUR 35IN FDA UDI
- Model / Reference
- 35EY FDA UDI
- Description
- MICROBORE EXT SET BIFUR 35IN FDA UDI
Identifiers
- Catalog Number
- 35EY FDA UDI
- Primary DI / UDI-DI
- 10192253007145 FDA UDI
- FDA Product Code
- KNT FDA UDI
- GMDN Term
- Enteral tube extension, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5980 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
- Length — 35 Inch FDA UDI
Category: Enteral tube extension, single-use
Kangaroo by Cardinal Health 200, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Enteral tube extension, single-use.
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- Codan — CODAN US Corporation · Class II
- Codan — CODAN US Corporation · Class II
- AMT MiniONE Extension Set — Applied Medical Technology, Inc. · Class II
- Kangaroo — Cardinalhealth · 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 |
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Manufacturer
- Manufacturer
- Cardinal Health 200, LLC
Sources (1)
- FDA UDI 930e5b85-782e-4450-a61d-79a09d64239e 35 fields · synced Jun 8, 2026