← Back to catalogue

NeoConnect Syringe-to-Syringe Coupler

FDA UDI

Class I (US FDA UDI)

by Neomed, Inc.

Identity

Trade Name
NeoConnect Syringe-to-Syringe Coupler FDA UDI
Generic Name
Enteral feeding/medication connector, sterile FDA UDI
Device Name
NeoConnect Syringe-to-Syringe Coupler, Sterile Purple FDA UDI
Model / Reference
PCO-FNC FDA UDI
Description
NeoConnect Syringe-to-Syringe Coupler, Sterile Purple FDA UDI

Identifiers

Catalog Number
PCO-FNC FDA UDI
Primary DI / UDI-DI
00817584010567 FDA UDI
FDA Product Code
KYX FDA UDI
GMDN Term
Enteral feeding/medication connector, sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6430 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

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: Enteral feeding/medication connector, sterile

NeoConnect Syringe-to-Syringe Coupler by Neomed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Enteral feeding/medication connector, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Neomed, Inc.

Sources (1)

  • FDA UDI d3f9c6e6-9854-4d42-9e16-91215b997c76 35 fields · synced May 30, 2026