← Back to catalogue

Trilogy Active PAP Tube Port Adapter

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 1061398Model Trilogy Circuit Accessories

by Respironics Inc.

Identity

Trade Name
Trilogy Active PAP Tube Port Adapter EUDAMED
Trilogy FDA UDI
Generic Name
Ventilator breathing circuit, reusable FDA UDI
Device Name
Trilogy Ventilator Active Positive Airway Pressure (PAP) Tubing Port Adapter FDA UDI
Model / Reference
Trilogy Circuit Accessories EUDAMED
1061398 EUDAMED
Trilogy Active PAP Tube Port Adapter FDA UDI
Description
Trilogy Ventilator Active Positive Airway Pressure (PAP) Tubing Port Adapter FDA UDI

Identifiers

Catalog Number
1061398 FDA UDI
Primary DI / UDI-DI
00606959043169 EUDAMEDFDA UDI
Basic UDI-DI
B-00606959043169 EUDAMED
FDA Product Code
CBK FDA UDI
EMDN Code
R02010199 STANDARD BREATHING CIRCUITS - OTHER EUDAMED
GMDN Term
Ventilator breathing circuit, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
868.5895 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Trilogy Active PAP Tube Port Adapter by Respironics Inc. — Class IIa — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (2)

  • EUDAMED 43a5d222-759d-460d-ac7d-ff2ab7b2b84c 61 fields · synced Jul 10, 2026
  • FDA UDI 97f7273b-232a-468e-a65f-17deab1afc69 36 fields · synced May 29, 2026