eudamed_udi Primary ID: 08698619571862

ILGAZ (UDI 08698619571862)

Manufactured by ONGUN TEKSTİL SAN. TİC. A.Ş.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The ILGAZ (Model/Catalog Number: O.T.M.193) is a medical device manufactured by ONGUN TEKSTİL SAN. TİC. A.Ş.. This product is indexed under FDA Product Code / Category Classification M0201020102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: O.T.M.193
Product Code / EMDN: M0201020102
Device Name: ABDOMINAL COMPRESS 40 × 40 CM 12 PLY
Database Sync Date: 2026-08-09 16:30:09

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 ILGAZ?

The registered manufacturer of record for ILGAZ is ONGUN TEKSTİL SAN. TİC. A.Ş..

What is the Primary UDI-DI identifier for ILGAZ?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08698619571862.

What classification code is assigned to this device?

This device is registered under product classification code M0201020102.

Similar Classification Devices (M0201020102)

Other Devices by ONGUN TEKSTİL SAN. TİC. A.Ş.

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