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Invacare HomeFill Foam Cabinet Filter

FDA UDI

Class I (US FDA UDI)

by SUNSET HEALTHCARE SOLUTIONS, Inc.

Identity

Trade Name
Invacare HomeFill Foam Cabinet Filter FDA UDI
Generic Name
Anaesthesia conduction filter FDA UDI
Device Name
Invacare HomeFill Foam Cabinet Filter (1/pack) FDA UDI
Model / Reference
OF9003-1 FDA UDI
Description
Invacare HomeFill Foam Cabinet Filter (1/pack) FDA UDI

Identifiers

Catalog Number
OF9003-1 FDA UDI
Primary DI / UDI-DI
00848530050986 FDA UDI
FDA Product Code
JRL FDA UDI
GMDN Term
Anaesthesia conduction filter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 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

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Anaesthesia conduction filter

Invacare HomeFill Foam Cabinet Filter by SUNSET HEALTHCARE SOLUTIONS, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthesia conduction filter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a9658689-acb3-484c-9e79-32dfc823922f 35 fields · synced May 29, 2026