Identity
- Trade Name
- NeoConnect Straw FDA UDI
- Generic Name
- Nasoenteral tube FDA UDI
- Device Name
- NeoConnect 3" (8 cm) Large Bore Sampling Straw with ENFit Connector, Orange FDA UDI
- Model / Reference
- EXT-3STBNC FDA UDI
- Description
- NeoConnect 3" (8 cm) Large Bore Sampling Straw with ENFit Connector, Orange FDA UDI
Identifiers
- Catalog Number
- EXT-3STNC FDA UDI
- Primary DI / UDI-DI
- 00817584013315 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
NeoConnect Straw 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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- PVC Feeding Tube — Avanos Medical, Inc. · Class II
- 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 58ef85f8-d982-41c5-9b86-030fa5476a85 35 fields · synced Jun 8, 2026