Identity

Trade Name
Oxygen Kit FDA UDI
Generic Name
Oxygen administration kit FDA UDI
Device Name
Oxygen Kit FDA UDI
Model / Reference
AELI010O2KIT FDA UDI
Description
Oxygen Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00848530089870 FDA UDI
GMDN Term
Oxygen administration kit FDA UDI

Classification

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. — 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

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Manufacturer

Sources (1)

  • FDA UDI f9dde677-64f7-42e7-abd3-a710c27fdf55 34 fields · synced Jun 6, 2026