eudamed_udi Primary ID: 08436035523931

Datospir Aira T (UDI 08436035523931)

Manufactured by SIBEL SAU

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Datospir Aira T (Model/Catalog Number: 09885) is a medical device manufactured by SIBEL SAU. This product is indexed under FDA Product Code / Category Classification Z12150101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 09885
Product Code / EMDN: Z12150101
Device Name: Datospir Aira
Database Sync Date: 2026-08-09 16:51:38

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 Datospir Aira T?

The registered manufacturer of record for Datospir Aira T is SIBEL SAU.

What is the Primary UDI-DI identifier for Datospir Aira T?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08436035523931.

What classification code is assigned to this device?

This device is registered under product classification code Z12150101.

Similar Classification Devices (Z12150101)

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