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MaxFlo2

FDA UDI

Class II (US FDA UDI)

by Maxtec, Inc.

Identity

Trade Name
MaxFlo2 FDA UDI
Generic Name
Oxygen/air breathing gas mixer, hospital FDA UDI
Device Name
MaxFlo2 High Flow with DISS Fitting FDA UDI
Model / Reference
High Flow DISS FDA UDI
Description
MaxFlo2 High Flow with DISS Fitting FDA UDI

Identifiers

Catalog Number
R223P02 FDA UDI
Primary DI / UDI-DI
00853061006029 FDA UDI
FDA Product Code
BZR FDA UDI
GMDN Term
Oxygen/air breathing gas mixer, hospital FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5330 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Weight — 2.4 Pound FDA UDI
Depth — 4.7 Inch FDA UDI
Width — 3.9 Inch FDA UDI
Height — 8.2 Inch FDA UDI

MaxFlo2 by Maxtec, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Maxtec, Inc.

Sources (1)

  • FDA UDI adb62919-0230-4aa1-8b9e-249c9371c63b 38 fields · synced Jun 8, 2026