← Back to catalogue

Pegasus

FDA UDI

Class I (US FDA UDI)

by Pegasus Research Corp.

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 UDI
Outer Diameter — 2 Inch FDA UDI
Weight — .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

Similar devices

Also classified as Oxygen administration tubing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Sources (1)

  • FDA UDI 37a9759c-8c8c-4057-a3a3-beb7493d9a03 35 fields · synced Jun 8, 2026