← Back to catalogue

Pacific Medico

FDA UDI

Class II (US FDA UDI)

by Pegasus Research Corp.

Identity

Trade Name
PACIFIC MEDICO FDA UDI
Generic Name
Inspiratory line humidification chamber, single-use FDA UDI
Device Name
HUMIDIFICATION CHAMBER, 500ML, 20/CASE FDA UDI
Model / Reference
PMC-500M FDA UDI
Description
HUMIDIFICATION CHAMBER, 500ML, 20/CASE FDA UDI

Identifiers

Catalog Number
PMC-500M FDA UDI
Primary DI / UDI-DI
00612223321024 FDA UDI
FDA Product Code
BTT FDA UDI
GMDN Term
Inspiratory line humidification chamber, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5450 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

No

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

No

FDA UDI

Dimensions & Sizes

Size
Height — 4.5 Inch FDA UDI
Outer Diameter — 4.9 Inch FDA UDI

Category: Inspiratory line humidification chamber, single-use

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

Similar devices

Also classified as Inspiratory line humidification chamber, single-use.

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

Manufacturer
Pegasus Research Corp.

Sources (1)

  • FDA UDI dac44520-d5c4-4fdd-9204-088fd703d8ec 35 fields · synced May 30, 2026