eudamed_udi Primary ID: 08436035523887

Datospir Touch Diagnostic-D (UDI 08436035523887)

Manufactured by SIBEL SAU

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Datospir Touch Diagnostic-D (Model/Catalog Number: 09880) 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: 09880
Product Code / EMDN: Z12150101
Device Name: Datospir Touch
Database Sync Date: 2026-08-09 16:45:58

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 Touch Diagnostic-D?

The registered manufacturer of record for Datospir Touch Diagnostic-D is SIBEL SAU.

What is the Primary UDI-DI identifier for Datospir Touch Diagnostic-D?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08436035523887.

What classification code is assigned to this device?

This device is registered under product classification code Z12150101.

Similar Classification Devices (Z12150101)

Other Devices by SIBEL SAU

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