Identity
- Trade Name
- Nexus TKO® FDA UDI
- Generic Name
- Intravenous administration tubing extension set FDA UDI
- Device Name
- Quadfurcated Extension Set with Nexus TKO®-6P, 60” Ultramicrobore Leg and 40” Spike Leg with Dual Check Valve and Nexus NIS®-6P FDA UDI
- Model / Reference
- P6880N FDA UDI
- Description
- Quadfurcated Extension Set with Nexus TKO®-6P, 60” Ultramicrobore Leg and 40” Spike Leg with Dual Check Valve and Nexus NIS®-6P FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10815879021677 FDA UDI
- FDA Product Code
- FPA FDA UDILHI FDA UDI
- GMDN Term
- Intravenous administration tubing extension set FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5440 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
Category: Intravenous administration tubing extension setFluid transfer set, general-purpose
Nexus TKO® by Nexus Medical, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Nexus Medical, LLC
Sources (1)
- FDA UDI 1d9dfb5f-693e-435a-b442-04d5588c6182 34 fields · synced Jun 1, 2026