← Back to catalogue

CPAP Filter

FDA UDI

Class I (US FDA UDI)

by SUNSET HEALTHCARE SOLUTIONS, Inc.

Identity

Trade Name
CPAP Filter FDA UDI
Generic Name
CPAP/BPAP unit ambient air filter, reusable FDA UDI
Device Name
Resmed S-9 CPAP Hypo Allergenic Filter - 50/Pack FDA UDI
Model / Reference
AVIT007CF2107HA-50PL FDA UDI
Description
Resmed S-9 CPAP Hypo Allergenic Filter - 50/Pack FDA UDI

Identifiers

Primary DI / UDI-DI
00848530083014 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

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

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI fd7c4e25-797e-46c6-8c58-c9045a7a6bfd 34 fields · synced May 30, 2026