Identity

Trade Name
RESO2KITAK FDA UDI
Generic Name
Oxygen administration kit FDA UDI
Device Name
This Kit Contains: 2 RES1107 Adult Cannula with 7ft Tube, 1 RES3007G Oxygen Tubing — 7ft — Green, 1 RES3025G Oxygen Tubing — 25ft — Green, 1 RES018 Tubing Connector with Swivel, 1 RES037 Water Trap, 1 RES050 Bubble Humidifier 6psi\, 1 RES032 Cylinder Wrench, 1 RES003 Oxygen In Use Sign, 1 HUM008L Humidifer Connector 21in FDA UDI
Model / Reference
RESO2KITAK FDA UDI
Description
This Kit Contains: 2 RES1107 Adult Cannula with 7ft Tube, 1 RES3007G Oxygen Tubing — 7ft — Green, 1 RES3025G Oxygen Tubing — 25ft — Green, 1 RES018 Tubing Connector with Swivel, 1 RES037 Water Trap, 1 RES050 Bubble Humidifier 6psi\, 1 RES032 Cylinder Wrench, 1 RES003 Oxygen In Use Sign, 1 HUM008L Humidifer Connector 21in FDA UDI

Identifiers

Catalog Number
RESO2KITAK FDA UDI
Primary DI / UDI-DI
00848530081812 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

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

Reso2kitak 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 dd344182-1dd2-4224-8be5-e8abe9d8aa93 35 fields · synced May 31, 2026