← Back to catalogue

NeoConnect Oral Administration Tip

FDA UDI

Class I (US FDA UDI)

by Neomed, Inc.

Identity

Trade Name
NeoConnect Oral Administration Tip FDA UDI
Generic Name
Oral liquid dose dispenser cabinet FDA UDI
Device Name
NeoConnect DoseMate, Oral Administration Tip, Sterile, Purple FDA UDI
Model / Reference
POA-TNC FDA UDI
Description
NeoConnect DoseMate, Oral Administration Tip, Sterile, Purple FDA UDI

Identifiers

Catalog Number
POA-TNC FDA UDI
Primary DI / UDI-DI
00817584011038 FDA UDI
FDA Product Code
KYX FDA UDI
GMDN Term
Oral liquid dose dispenser cabinet 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: Oral liquid dose dispenser cabinet

NeoConnect Oral Administration Tip by Neomed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oral liquid dose dispenser cabinet.

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 289ce20f-0dbc-499f-be05-9f9dcd6f4876 35 fields · synced Jun 8, 2026