GUDIDData
eudamed_udi Primary ID: 08697613216571

Chest Roll, Gel, Adult (UDI 08697613216571)

Manufactured by UZUMCU MEDICAL EQUIPMENT and GAS SYSTEMS

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Chest Roll, Gel, Adult - Primary ID 08697613216571

Device Regulatory Overview

The Chest Roll, Gel, Adult (Model/Catalog Number: 11.1014) is a medical device manufactured by UZUMCU MEDICAL EQUIPMENT and GAS SYSTEMS. This product is indexed under FDA Product Code / Category Classification Z12011202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
11.1014
Product Code / EMDN
Z12011202
Device Name
Obesity Operating TableElectromechanical
Database Sync Date
2026-08-09 16:44:55

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 Chest Roll, Gel, Adult?

The registered manufacturer of record for Chest Roll, Gel, Adult is UZUMCU MEDICAL EQUIPMENT and GAS SYSTEMS.

What is the Primary UDI-DI identifier for Chest Roll, Gel, Adult?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08697613216571.

What classification code is assigned to this device?

This device is registered under product classification code Z12011202.

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