Identity
- Trade Name
- NeoConnect Pharmacy Syringe FDA UDI
- Generic Name
- ENFit oral/enteral syringe, single-use FDA UDI
- Device Name
- 12mL NeoConnect Pharmacy Syringe, Amber, White Print, Sterile FDA UDI
- Model / Reference
- BA-S12NC-S FDA UDI
- Description
- 12mL NeoConnect Pharmacy Syringe, Amber, White Print, Sterile FDA UDI
Identifiers
- Catalog Number
- BA-S12NC-S FDA UDI
- Primary DI / UDI-DI
- 00817584012486 FDA UDI
- FDA Product Code
- PNR FDA UDI
- GMDN Term
- ENFit oral/enteral syringe, 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
Category: ENFit oral/enteral syringe, single-use
NeoConnect Pharmacy Syringe by Neomed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as ENFit oral/enteral syringe, single-use.
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- VYGON — Vygon Corp. · Class II
- BD UniVia — BECTON DICKINSON AND COMPANY · Class II
- VYGON — Vygon Corp. · 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 8f8dd001-e84d-4c22-aa8f-3b754204303b 35 fields · synced Jun 1, 2026