MAXIIa (UDI MAXIIa)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The MAXIIa (Model/Catalog Number: MAXIIa) is a medical device manufactured by Aei Technologies, Inc.. This product is indexed under FDA Product Code / Category Classification BZL within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MAXIIa
Product Code / EMDN: BZL
Device Name: Metabolic Measurement System
Database Sync Date: 2026-08-09 09:06:20

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of MAXIIa?

The registered manufacturer of record for MAXIIa is Aei Technologies, Inc..

What is the Primary UDI-DI identifier for MAXIIa?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MAXIIa.

What classification code is assigned to this device?

This device is registered under product classification code BZL.

Similar Classification Devices (BZL)

Other Devices by Aei Technologies, Inc.

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