GUDIDData
eudamed_udi Primary ID: 08680202285317

TYVEK STERİLİZASYON RULOSU 30CMX70M (UDI 08680202285317)

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 STERİLİZASYON RULOSU 30CMX70M - Primary ID 08680202285317

Device Regulatory Overview

The TYVEK STERİLİZASYON RULOSU 30CMX70M (Model/Catalog Number: TY3070) 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 S01020201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
TY3070
Product Code / EMDN
S01020201
Device Name
TYVEK STERİLİZASYON RULOSU 10CMX70M
Database Sync Date
2026-08-09 16:29:47

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 STERİLİZASYON RULOSU 30CMX70M?

The registered manufacturer of record for TYVEK STERİLİZASYON RULOSU 30CMX70M is SUDEMED TIBBİ ÜRÜNLER EMLAK İNŞAAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ.

What is the Primary UDI-DI identifier for TYVEK STERİLİZASYON RULOSU 30CMX70M?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08680202285317.

What classification code is assigned to this device?

This device is registered under product classification code S01020201.

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