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Face Mask, Medium Adult

FDA UDI

Class I (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Face Mask, Medium Adult FDA UDI
Generic Name
Anaesthesia face mask, single-use FDA UDI
Device Name
Face Mask, Medium Adult W/Hook Ring and Valve, Series 810 FDA UDI
Model / Reference
7-9811 FDA UDI
Description
Face Mask, Medium Adult W/Hook Ring and Valve, Series 810 FDA UDI

Identifiers

Primary DI / UDI-DI
00709078003691 FDA UDI
FDA Product Code
BSJ FDA UDI
GMDN Term
Anaesthesia face mask, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5550 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Anaesthesia face mask, single-use

Face Mask, Medium Adult by Westmed, Inc. — Class I — 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 cb7b232d-54c2-4531-9410-e42f3b417ba6 33 fields · synced May 30, 2026