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Neomed*

FDA UDI

Class II (US FDA UDI)

by Avanos Medical, Inc.

Identity

Trade Name
NEOMED* FDA UDI
Generic Name
Cardiopulmonary bypass system air bubble/fluid level detector FDA UDI
Device Name
LN2215 Lumbar Needle, 22G x 1.5" Spinal Needle FDA UDI
Model / Reference
LN2215 FDA UDI
Description
LN2215 Lumbar Needle, 22G x 1.5" Spinal Needle FDA UDI

Identifiers

Catalog Number
LN2215 FDA UDI
Primary DI / UDI-DI
00350770003351 FDA UDI
FDA Product Code
PWY FDA UDI
GMDN Term
Cardiopulmonary bypass system air bubble/fluid level detector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 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

No

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: Cardiopulmonary bypass system air bubble/fluid level detector

Neomed* by Avanos Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiopulmonary bypass system air bubble/fluid level detector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Avanos Medical, Inc.

Sources (1)

  • FDA UDI 3c16ad0d-5a69-4031-aaca-bff0cca85229 35 fields · synced Jun 9, 2026