Identity
- Trade Name
- NeoMed Enteral Extension Set FDA UDI
- Generic Name
- Nasoenteral tube FDA UDI
- Device Name
- 40" (102 cm) PVC Enteral Extension Set, Enteral Only, Large Bore FDA UDI
- Model / Reference
- NM-40ENENB FDA UDI
- Description
- 40" (102 cm) PVC Enteral Extension Set, Enteral Only, Large Bore FDA UDI
Identifiers
- Catalog Number
- NM-40ENENB FDA UDI
- Primary DI / UDI-DI
- 00817584010970 FDA UDI
- FDA Product Code
- KNT FDA UDI
- GMDN Term
- Nasoenteral tube 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
Category: Nasoenteral tube
NeoMed Enteral Extension Set by Neomed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Nasoenteral tube.
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- ENFit Extension Set — Avanos Medical, Inc. · Class II
- Argyle — Cardinal Health 200, LLC · Class II
- ENFit Syringe — Avanos Medical, Inc. · Class II
- Kangaroo — Cardinalhealth · Class II
- NutraGlide Nasal Feeding Tube — Applied Medical Technology, 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 |
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Manufacturer
- Manufacturer
- Neomed, Inc.
Sources (1)
- FDA UDI ab59b7b6-e862-4c6b-b479-c13bae9b8de6 35 fields · synced Jun 8, 2026