Identity
- Trade Name
- NeoMed Straw FDA UDI
- Generic Name
- Nasoenteral tube FDA UDI
- Device Name
- 6" (15 cm) PVC Sampling Straw, Enteral Only, Large Bore, Purple FDA UDI
- Model / Reference
- PNM-6ENSTB FDA UDI
- Description
- 6" (15 cm) PVC Sampling Straw, Enteral Only, Large Bore, Purple FDA UDI
Identifiers
- Catalog Number
- PNM-6ENSTB FDA UDI
- Primary DI / UDI-DI
- 00817584012905 FDA UDI
- FDA Product Code
- ILC FDA UDI
- GMDN Term
- Nasoenteral tube FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5050 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
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
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 Straw by Neomed, Inc. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Neomed, Inc.
Sources (1)
- FDA UDI b93ff1f9-b074-4aed-8715-1a79e95a834d 35 fields · synced May 30, 2026