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Trilogy Active Flow Exhalation Circuit Adult
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 1068837Model Trilogy Circuit Accessories
Identity
- Trade Name
- Trilogy Active Flow Exhalation Circuit Adult EUDAMEDBiPAP A40 EFL FDA UDI
- Generic Name
- Ventilator breathing circuit, reusable FDA UDI
- Device Name
- Trilogy Ventilator - Active Flow Exhalation Patient Circuit, Adult FDA UDI
- Model / Reference
- Trilogy Circuit Accessories EUDAMED1068837 EUDAMEDTrilogy Active Flow Exhalation Circuit, Adult FDA UDI
- Description
- Trilogy Ventilator - Active Flow Exhalation Patient Circuit, Adult FDA UDI
Identifiers
- Catalog Number
- 1068837 FDA UDI
- Primary DI / UDI-DI
- 00606959005211 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00606959005211 EUDAMED
- FDA Product Code
- CBK FDA UDI
- EMDN Code
- Z12150180 SPIROMETRY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
- GMDN Term
- Ventilator breathing circuit, reusable FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass 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 Flow Exhalation Circuit Adult 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-00606959005211 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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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 0e319bff-fec6-4bca-afb3-adbf388642c6 61 fields · synced Jul 14, 2026
- FDA UDI 13522cea-b99e-4aa6-abed-002cbcfea500 36 fields · synced May 30, 2026