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Trilogy 200

by Respironics Inc.

Ref 1032802Model Trilogy 200

Trilogy 200 (1032802) is a Class IIb device made by Respironics Inc., registered in EUDAMED on 29 Sep 2025 (Basic UDI-DI B-00606959429567), withdrawn as of 25 Oct 2026.

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDD, withdrawn

Ended

Withdrawn

Date not published (CE MDD)

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-00606959429567 Basic UDI-DI 00606959429567UDI-DIDate29 Sep 2025RegisteredStatusWithdrawn No longer placed on the EU market

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Withdrawn

Specification

EUDAMED

Model / reference
Trilogy 200, 1032802
Primary DI / UDI-DI
00606959429567
Basic UDI-DI
B-00606959429567
EMDN code
Z12030103 Pulmonary ventilators for non–hospital use
Device class
Class IIb
EU registration type
Legacy device (under a directive)
EU market of registration
Austria

Manufacturer details

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

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Properties

Other properties (12, all answered No)