MAXAIR (UDI 2600-02-PR)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The MAXAIR (Model/Catalog Number: 2600-02-PR) is a medical device manufactured by Syntech, Int'l Inc.. This product is indexed under FDA Product Code / Category Classification LYU within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 2600-02-PR
Product Code / EMDN: LYU
Device Name: CHARGER
Database Sync Date: 2026-08-09 09:37:37

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 MAXAIR?

The registered manufacturer of record for MAXAIR is Syntech, Int'l Inc..

What is the Primary UDI-DI identifier for MAXAIR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2600-02-PR.

What classification code is assigned to this device?

This device is registered under product classification code LYU.

Similar Classification Devices (LYU)

Other Devices by Syntech, Int'l Inc.

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