Identity
- Trade Name
- PEGASUS FDA UDI
- Generic Name
- Oxygen administration tubing FDA UDI
- Device Name
- FLO2 HIGH FLOW OXYGEN DILUTER, ADULT KIT FDA UDI
- Model / Reference
- P6000 FDA UDI
- Description
- FLO2 HIGH FLOW OXYGEN DILUTER, ADULT KIT FDA UDI
Identifiers
- Catalog Number
- P6000 FDA UDI
- Primary DI / UDI-DI
- 00612223060015 FDA UDI
- FDA Product Code
- BYF FDA UDI
- GMDN Term
- Oxygen administration tubing FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5600 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 6 Feet FDA UDIOuter Diameter — 2 Inch FDA UDIWeight — .4 Pound FDA UDI
Category: Oxygen administration tubing
Pegasus by Pegasus Research Corp. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Pegasus Research Corp.
Sources (1)
- FDA UDI 37a9759c-8c8c-4057-a3a3-beb7493d9a03 35 fields · synced Jun 8, 2026