OxyGo Inline Water Trap, For Oxygen Delivery

FDA UDI

Class II (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name: OxyGo Inline Water Trap, For Oxygen Delivery FDA UDI
Generic Name: Breathing circuit condensate trap, reusable FDA UDI
Device Name: Condensate Collection Trap FDA UDI
Model / Reference: 1425-1013 FDA UDI
Description: Condensate Collection Trap FDA UDI

Identifiers

Primary DI / UDI-DI: 00709078005947 FDA UDI
510(k) Number: K954271 FDA UDI
FDA Product Code: CAW FDA UDI
GMDN Term: Breathing circuit condensate trap, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5440 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

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: Breathing circuit condensate trap, reusable

OxyGo Inline Water Trap, For Oxygen Delivery by Westmed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Breathing circuit condensate trap, reusable.

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Expression MR KIT, DISPOSABLE WATER TRAP, 3160 — Philips DS North America LLC · Class II
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Cleared under the same submission

K954271 also covers:

Inline Water Trap — WESTMED, INC.
Water Trap — 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 II	Pending data

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Manufacturer

Manufacturer: Westmed, Inc.

Sources (1)

FDA UDI 4f7762b9-737c-45da-afca-2104122d77fb 34 fields · synced May 30, 2026