gudid Primary ID: 102100

Aira (UDI 102100)

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: 102100) is a medical device manufactured by AIRA, LLC. This product is indexed under FDA Product Code / Category Classification EFT within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 102100
Product Code / EMDN: EFT
Device Name: Ultrasonic Cleaning Tablets 64pcs/Bx - 10 Bx/CS
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 102100.

What classification code is assigned to this device?

This device is registered under product classification code EFT.

Similar Classification Devices (EFT)

Other Devices by AIRA, LLC

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