← Back to catalogue

Oxygen Kit

FDA UDI

Class II (US FDA UDI)

by SUNSET HEALTHCARE SOLUTIONS, Inc.

Identity

Trade Name
Oxygen Kit FDA UDI
Generic Name
Oxygen administration kit FDA UDI
Device Name
Oxygen Kit This kit contains: (2) RES3025, (6) RES1107, (2) RES003, (3) RES018 FDA UDI
Model / Reference
ABLA002O2KIT FDA UDI
Description
Oxygen Kit This kit contains: (2) RES3025, (6) RES1107, (2) RES003, (3) RES018 FDA UDI

Identifiers

Primary DI / UDI-DI
00848530105150 FDA UDI
FDA Product Code
OGL FDA UDI
GMDN Term
Oxygen administration kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5655 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

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: Oxygen administration kit

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

Similar devices

Also classified as Oxygen administration kit.

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 58059663-a2e0-48fc-8a18-cc5d8f3b36ba 34 fields · synced Jun 8, 2026