Trilogy

FDA UDI

Class II (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name: Trilogy FDA UDI
Generic Name: Portable electric ventilator FDA UDI
Device Name: Trilogy 202 Ventilator, Canada FDA UDI
Model / Reference: Trilogy 202 Ventilator, Canada FDA UDI
Description: Trilogy 202 Ventilator, Canada FDA UDI

Identifiers

Catalog Number: CA1040000 FDA UDI
Primary DI / UDI-DI: 00606959022799 FDA UDI
510(k) Number: K093905 FDA UDI
FDA Product Code: DQA FDA UDI
CBK FDA UDI
GMDN Term: Portable electric ventilator FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.2700 FDA UDI
868.5895 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

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

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Portable electric ventilator

Trilogy by Respironics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K093905 also covers:

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: Respironics, Inc.

Sources (1)

FDA UDI c5e28519-00c8-4627-8f00-9e90d97899d9 37 fields · synced May 30, 2026