GUDIDData
eudamed_udi Primary ID: 08680202282149

TYVEK BÖLMELİ STERİLİZASYON POŞETİ HEADERBAG 30CM X 70CM (UDI 08680202282149)

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 TYVEK BÖLMELİ STERİLİZASYON POŞETİ HEADERBAG 30CM X 70CM - Primary ID 08680202282149

Device Regulatory Overview

The TYVEK BÖLMELİ STERİLİZASYON POŞETİ HEADERBAG 30CM X 70CM (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 S010301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
YOK
Product Code / EMDN
S010301
Device Name
TYVEK STERİLİZASYON RULOSU 10CMX70M
Database Sync Date
2026-08-09 16:29:22

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 TYVEK BÖLMELİ STERİLİZASYON POŞETİ HEADERBAG 30CM X 70CM?

The registered manufacturer of record for TYVEK BÖLMELİ STERİLİZASYON POŞETİ HEADERBAG 30CM X 70CM is SUDEMED TIBBİ ÜRÜNLER EMLAK İNŞAAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ.

What is the Primary UDI-DI identifier for TYVEK BÖLMELİ STERİLİZASYON POŞETİ HEADERBAG 30CM X 70CM?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08680202282149.

What classification code is assigned to this device?

This device is registered under product classification code S010301.

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