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Respironics Solo, Aria LX, Virtuoso LX, REMstar LX Style Ultrafine Filters

FDA UDI

Class I (US FDA UDI)

by SUNSET HEALTHCARE SOLUTIONS, Inc.

Identity

Trade Name
Respironics Solo, Aria LX, Virtuoso LX, REMstar LX Style Ultrafine Filters FDA UDI
Generic Name
CPAP/BPAP unit ambient air filter, reusable FDA UDI
Device Name
Respironics Solo, Aria LX, Virtuoso LX, REMstar LX Style Ultrafine Filters (2/pack) FDA UDI
Model / Reference
CF1002-2 FDA UDI
Description
Respironics Solo, Aria LX, Virtuoso LX, REMstar LX Style Ultrafine Filters (2/pack) FDA UDI

Identifiers

Catalog Number
CF1002-2 FDA UDI
Primary DI / UDI-DI
00848530030117 FDA UDI
FDA Product Code
JRL FDA UDI
GMDN Term
CPAP/BPAP unit ambient air filter, reusable 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: CPAP/BPAP unit ambient air filter, reusable

Respironics Solo, Aria LX, Virtuoso LX, REMstar LX Style Ultrafine Filters by SUNSET HEALTHCARE SOLUTIONS, Inc. — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as CPAP/BPAP unit ambient air filter, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4d6375f8-06bf-412c-b05b-28c545897664 35 fields · synced May 30, 2026