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Eitan Medical

FDA UDI

Class II (US FDA UDI)

by Optumhealth Care Solutions, Inc.

Identity

Trade Name
Eitan Medical FDA UDI
Generic Name
Bedside infusion pump, single-channel FDA UDI
Device Name
Avoset-Optum Homecare Infusion FDA UDI
Model / Reference
Pump Avoset Infusion FDA UDI
Description
Avoset-Optum Homecare Infusion FDA UDI

Identifiers

Catalog Number
AAA-00171 FDA UDI
Primary DI / UDI-DI
00862492000353 FDA UDI
FDA Product Code
FRN FDA UDI
GMDN Term
Bedside infusion pump, single-channel FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5725 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Bedside infusion pump, single-channel

Eitan Medical by Optumhealth Care Solutions, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bedside infusion pump, single-channel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f944a90d-91cd-4eac-8463-dc0f45d248ab 34 fields · synced May 29, 2026