Transport Kit with Adult Elongated Oxygen Mast

FDA UDI

Class I (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name: Transport Kit with Adult Elongated Oxygen Mast FDA UDI
Generic Name: Oxygen administration tubing FDA UDI
Model / Reference: 9439 FDA UDI

Identifiers

Primary DI / UDI-DI: 00709078004780 FDA UDI
510(k) Number: K904538 FDA UDI
FDA Product Code: CAI FDA UDI
GMDN Term: Oxygen administration tubing FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.5240 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Oxygen administration tubing

Transport Kit with Adult Elongated Oxygen Mast by Westmed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K904538 also covers:

Anapod™ Humi-therm Heated and Humidified Wick Breathing Circuit — WESTMED, INC.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Westmed, Inc.

Sources (1)

FDA UDI 9600dae2-8883-4f02-b547-a15dae77083a 33 fields · synced Jun 8, 2026