MicroBlender

FDA UDI

Class II (US FDA UDI)

by Maxtec, Inc.

Identity

Trade Name: MicroBlender FDA UDI
Generic Name: Oxygen/air breathing gas mixer, hospital FDA UDI
Device Name: Low Flow FDA UDI
Model / Reference: R219P24 FDA UDI
Description: Low Flow FDA UDI

Identifiers

Primary DI / UDI-DI: 00817770020714 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: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Oxygen/air breathing gas mixer, hospital

MicroBlender by Maxtec, Inc. — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Maxtec, Inc.

Sources (1)

FDA UDI 90f2d9e8-63cd-4167-97dd-1e1791b30728 33 fields · synced May 30, 2026