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Trilogy 202 Ventilator International

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 1040000

by Respironics Inc.

Identity

Trade Name
Trilogy 202 Ventilator International EUDAMED
Trilogy FDA UDI
Generic Name
Portable electric ventilator FDA UDI
Device Name
Trilogy 202/O2 EUDAMED
Trilogy 202 Ventilator, International FDA UDI
Model / Reference
1040000 EUDAMED
Trilogy 202 Ventilator International FDA UDI
Description
Trilogy 202 Ventilator, International FDA UDI

Identifiers

Catalog Number
1040000 FDA UDI
Primary DI / UDI-DI
00606959022706 EUDAMEDFDA UDI
Basic UDI-DI
B-00606959022706 EUDAMED
510(k) Number
K093905 FDA UDI
FDA Product Code
CBK FDA UDI
DQA FDA UDI
EMDN Code
Z12030103 PULMONARY VENTILATORS FOR NON–HOSPITAL USE EUDAMED
GMDN Term
Portable electric ventilator FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
868.5895 FDA UDI
870.2700 FDA UDI
Market of Registration
Austria EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Trilogy 202 Ventilator International by Respironics, Inc. — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Respironics Inc.
EUDAMED SRN
US-MF-000002301
Authorised Representative
Respironics Deutschland GmbH & Co.KG DE-AR-000006164

Sources (2)

  • EUDAMED dc5432e1-498a-479e-ba5f-55d1033b49ec 61 fields · synced Jun 17, 2026
  • FDA UDI 47a7dd37-396a-4eb6-b631-e6eef2234d65 37 fields · synced May 30, 2026