← Back to catalogue

Oxygen Mask

FDA UDI

Class I (US FDA UDI)

by SUNSET HEALTHCARE SOLUTIONS, Inc.

Identity

Trade Name
Oxygen Mask FDA UDI
Generic Name
Aerosol face mask, rebreathing, single-use FDA UDI
Device Name
High Concentration Venturi Style Oxygen Delivery System FDA UDI
Model / Reference
RES2401 FDA UDI
Description
High Concentration Venturi Style Oxygen Delivery System FDA UDI

Identifiers

Primary DI / UDI-DI
00848530096298 FDA UDI
FDA Product Code
BYG FDA UDI
GMDN Term
Aerosol face mask, rebreathing, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5580 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

Yes

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: Aerosol face mask, rebreathing, single-use

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

Similar devices

Also classified as Aerosol face mask, rebreathing, single-use.

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 57788bf6-a529-462c-85b9-9159a41616cd 34 fields · synced May 30, 2026