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Neomed*

FDA UDI

Class I (US FDA UDI)

by Avanos Medical, Inc.

Identity

Trade Name
NEOMED* FDA UDI
Generic Name
Oral liquid dose dispenser cabinet FDA UDI
Device Name
ENFit DoseMate DL Sterile Purp FDA UDI
Model / Reference
POA-TNCL FDA UDI
Description
ENFit DoseMate DL Sterile Purp FDA UDI

Identifiers

Catalog Number
POA-TNCL FDA UDI
Primary DI / UDI-DI
00350770000473 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

Neomed* by Avanos Medical, 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

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Manufacturer

Sources (1)

  • FDA UDI 77df0047-d828-4054-827d-a5418d677900 35 fields · synced Jun 9, 2026