Identity
- Trade Name
- Trilogy FDA UDI
- Generic Name
- Ventilator breathing circuit, reusable FDA UDI
- Device Name
- Trilogy Ventilator Passive Exhalation Patient Circuit, Adult FDA UDI
- Model / Reference
- Trilogy Passive Exhalation Circuit, Adult FDA UDI
- Description
- Trilogy Ventilator Passive Exhalation Patient Circuit, Adult FDA UDI
Identifiers
- Catalog Number
- 1052066 FDA UDI
- Primary DI / UDI-DI
- 00606959026155 FDA UDI
- FDA Product Code
- CBK FDA UDI
- GMDN Term
- Ventilator breathing circuit, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5895 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
Category: Ventilator breathing circuit, reusable
Trilogy by Respironics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Respironics, Inc.
Sources (1)
- FDA UDI 11493e71-2b58-456c-ad2e-bafdcd978273 36 fields · synced May 30, 2026