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144"Adult Circuit, Bi-Wye

FDA UDI

Class II (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
144"Adult Circuit, Bi-Wye FDA UDI
Generic Name
Anaesthesia face mask, single-use FDA UDI
Device Name
144" Adult EXP, GSE, Wye w/GSP, Large Mask, 2LF, GSL, suction tube FDA UDI
Model / Reference
9579 FDA UDI
Description
144" Adult EXP, GSE, Wye w/GSP, Large Mask, 2LF, GSL, suction tube FDA UDI

Identifiers

Primary DI / UDI-DI
00709078003288 FDA UDI
FDA Product Code
CAH FDA UDI
GMDN Term
Anaesthesia face mask, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5260 FDA UDI
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

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Anaesthesia face mask, single-use

144"Adult Circuit, Bi-Wye by Westmed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthesia face mask, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI b0bb8838-b2da-46b1-8724-3708687c656f 34 fields · synced May 30, 2026