KREPE KAĞIT (STERİLİZASYON WRAP KAĞIDI) 60CMX60CM (UDI 08680202280053)
Manufactured by SUDEMED TIBBİ ÜRÜNLER EMLAK İNŞAAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ
Device Regulatory Overview
The KREPE KAĞIT (STERİLİZASYON WRAP KAĞIDI) 60CMX60CM (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 16:29:29
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of KREPE KAĞIT (STERİLİZASYON WRAP KAĞIDI) 60CMX60CM?
The registered manufacturer of record for KREPE KAĞIT (STERİLİZASYON WRAP KAĞIDI) 60CMX60CM is SUDEMED TIBBİ ÜRÜNLER EMLAK İNŞAAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ.
What is the Primary UDI-DI identifier for KREPE KAĞIT (STERİLİZASYON WRAP KAĞIDI) 60CMX60CM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08680202280053.
What classification code is assigned to this device?
This device is registered under product classification code S010301.
Similar Classification Devices (S010301)
Other Devices by SUDEMED TIBBİ ÜRÜNLER EMLAK İNŞAAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ
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