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Berman Oral Airway

FDA UDI

Class I (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Berman Oral Airway FDA UDI
Generic Name
Oesophageal-obturating/tracheal airway, single-use FDA UDI
Device Name
Standard Berman Oral Airway 100mm (Individually Bagged) (TwinMed) FDA UDI
Model / Reference
1002266 FDA UDI
Description
Standard Berman Oral Airway 100mm (Individually Bagged) (TwinMed) FDA UDI

Identifiers

Primary DI / UDI-DI
00709078014475 FDA UDI
FDA Product Code
CAE FDA UDI
GMDN Term
Oesophageal-obturating/tracheal airway, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5110 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: Oesophageal-obturating/tracheal airway, single-use

Berman Oral Airway by Westmed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oesophageal-obturating/tracheal airway, 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 8eeefe4d-7445-4c57-b872-d23e0c2047c0 33 fields · synced May 29, 2026