Aira (UDI 100546)

Manufactured by AIRA, LLC

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Aira (Model/Catalog Number: 100546) is a medical device manufactured by AIRA, LLC. This product is indexed under FDA Product Code / Category Classification FRG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 100546
Product Code / EMDN: FRG
Device Name: 3.25" x 11" - Paper/Blue Film Self-Sealing Sterilization Pouch
Database Sync Date: 2026-08-09 09:22:20

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 Aira?

The registered manufacturer of record for Aira is AIRA, LLC.

What is the Primary UDI-DI identifier for Aira?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 100546.

What classification code is assigned to this device?

This device is registered under product classification code FRG.

Similar Classification Devices (FRG)

Other Devices by AIRA, LLC

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