← Back to catalogue
Trilogy Evo, O2, EU
EUDAMEDFDA UDIClass IIb (EU MDR)
Ref EU2100X15BModel Trilogy Evo, O2, EU
Identity
- Trade Name
- Trilogy Evo, O2, EU EUDAMEDTrilogy FDA UDI
- Generic Name
- Portable electric ventilator FDA UDI
- Device Name
- Trilogy Evo Ventilator System with Oxygen Blending Module and Bluetooth, Europe FDA UDI
- Model / Reference
- Trilogy Evo, O2, EU EUDAMEDEU2100X15B EUDAMEDTrilogy Evo Ventilator with oxygen blending model, EU FDA UDI
- Description
- Trilogy Evo Ventilator System with Oxygen Blending Module and Bluetooth, Europe FDA UDI
Identifiers
- Catalog Number
- EU2100X15B FDA UDI
- Primary DI / UDI-DI
- 00606959055674 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00606959055674 EUDAMED
- FDA Product Code
- CBK FDA UDICCK FDA UDIDQA FDA UDI
- EMDN Code
- Z12030104 PORTABLE PULMONARY VENTILATORS EUDAMED
- GMDN Term
- Portable electric ventilator FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 868.5895 FDA UDI868.1400 FDA UDI870.2700 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
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Trilogy Evo, O2, EU 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-00606959055674 | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
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 (3)
- EUDAMED 024340dd-d225-4245-9bef-bef7260032a5 61 fields · synced Jun 19, 2026
- FDA UDI edfc1336-bbfa-46b6-b5c4-528e690a0040 35 fields · synced May 30, 2026
- EUDAMED 8ff5b0f4-24fd-462b-9b28-9a337fcaa94e 61 fields · synced Jun 19, 2026