GUDIDData
eudamed_udi Primary ID: 08680202286222

SMS KUMAŞ (WRAP) 90 CM X 90 CM (UDI 08680202286222)

Manufactured by SUDEMED TIBBİ ÜRÜNLER EMLAK İNŞAAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SMS KUMAŞ (WRAP) 90 CM X 90 CM - Primary ID 08680202286222

Device Regulatory Overview

The SMS KUMAŞ (WRAP) 90 CM X 90 CM (Model/Catalog Number: YOK) is a medical device manufactured by SUDEMED TIBBİ ÜRÜNLER EMLAK İNŞAAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification S010302 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
YOK
Product Code / EMDN
S010302
Device Name
TYVEK STERİLİZASYON RULOSU 10CMX70M
Database Sync Date
2026-08-09 16:28:48

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 SMS KUMAŞ (WRAP) 90 CM X 90 CM?

The registered manufacturer of record for SMS KUMAŞ (WRAP) 90 CM X 90 CM is SUDEMED TIBBİ ÜRÜNLER EMLAK İNŞAAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ.

What is the Primary UDI-DI identifier for SMS KUMAŞ (WRAP) 90 CM X 90 CM?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08680202286222.

What classification code is assigned to this device?

This device is registered under product classification code S010302.

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