GUDIDData
eudamed_udi Primary ID: 08698863812568

DEM (UDI 08698863812568)

Manufactured by Foras Bilgisayar Elektronik Medikal San. ve Tic. Ltd. Şti.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DEM - Primary ID 08698863812568

Device Regulatory Overview

The DEM (Model/Catalog Number: 2568) is a medical device manufactured by Foras Bilgisayar Elektronik Medikal San. ve Tic. Ltd. Şti.. This product is indexed under FDA Product Code / Category Classification Z12030102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
2568
Product Code / EMDN
Z12030102
Device Name
Breathing Machines
Database Sync Date
2026-08-09 18:36:41

Full Regulatory Attributes

🔒 Token Gated
{
    "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 DEM?

The registered manufacturer of record for DEM is Foras Bilgisayar Elektronik Medikal San. ve Tic. Ltd. Şti..

What is the Primary UDI-DI identifier for DEM?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08698863812568.

What classification code is assigned to this device?

This device is registered under product classification code Z12030102.

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