Pro-N20

FDA UDI

Class II (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name: Pro-N20 FDA UDI
Generic Name: Anaesthesia breathing circuit, single-use FDA UDI
Device Name: Pro-N20 Corrugated Patient Elbow Bifurcated Wye FDA UDI
Model / Reference: 9421 FDA UDI
Description: Pro-N20 Corrugated Patient Elbow Bifurcated Wye FDA UDI

Identifiers

Primary DI / UDI-DI: 00709078006739 FDA UDI
FDA Product Code: CAH FDA UDI
OFP FDA UDI
GMDN Term: Anaesthesia breathing circuit, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5260 FDA UDI
868.5240 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Anaesthesia breathing circuit, single-use

Pro-N20 by Westmed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 cff7b827-ffb4-4bcc-ae82-9ff9c7bf6247 33 fields · synced May 31, 2026