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NeoConnect Pharmacy Syringe

FDA UDI

Class II (US FDA UDI)

by Neomed, Inc.

Identity

Trade Name
NeoConnect Pharmacy Syringe FDA UDI
Generic Name
ENFit oral/enteral syringe, single-use FDA UDI
Device Name
1mL NeoConnect Pharmacy Syringe, Amber, White Print, Non-Sterile FDA UDI
Model / Reference
BA-S1NC FDA UDI
Description
1mL NeoConnect Pharmacy Syringe, Amber, White Print, Non-Sterile FDA UDI

Identifiers

Catalog Number
BA-S1NC FDA UDI
Primary DI / UDI-DI
20817584012305 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

No

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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neomed, Inc.

Sources (1)

  • FDA UDI 95b9d07b-6417-485a-8ea7-448fd70a05ee 35 fields · synced May 30, 2026