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Pegasus

FDA UDI

Class II (US FDA UDI)

by Pegasus Research Corp.

Identity

Trade Name
PEGASUS FDA UDI
Generic Name
Heated respiratory humidifier FDA UDI
Device Name
HUMIDIFIER HEATER BRACKET, VISION/PHILIPSV60 FIT FDA UDI
Model / Reference
P23001 FDA UDI
Description
HUMIDIFIER HEATER BRACKET, VISION/PHILIPSV60 FIT FDA UDI

Identifiers

Catalog Number
P23001 FDA UDI
Primary DI / UDI-DI
00612223230012 FDA UDI
510(k) Number
K880473 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Heated respiratory humidifier FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5630 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

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 5 Inch FDA UDI
Height — 2.5 Inch FDA UDI
Width — 2.8 Inch FDA UDI

Category: Heated respiratory humidifier

Pegasus by Pegasus Research Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Heated respiratory humidifier.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0ecbb05a-fbff-4858-a9f9-69444f3fe6aa 36 fields · synced Jun 7, 2026