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InLine Water Trap

FDA UDI

Class II (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
InLine Water Trap FDA UDI
Generic Name
Breathing circuit condensate trap, reusable FDA UDI
Device Name
Inline Water Trap For Oxygen Delivery FDA UDI
Model / Reference
1002277 FDA UDI
Description
Inline Water Trap For Oxygen Delivery FDA UDI

Identifiers

Primary DI / UDI-DI
00709078014062 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Breathing circuit condensate trap, reusable

InLine Water Trap by Westmed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Breathing circuit condensate trap, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI bd58dfd8-12b4-49d7-a31d-70a531031083 33 fields · synced May 30, 2026