STERİLİZASYON WRAP KAĞIDI 25 (±5) X 55 (±5)CM (UDI 08681744105071)
Manufactured by BAYTEKS TEKNİK TEKSTİL SAN. VE TİC. A.Ş.
Device Regulatory Overview
The STERİLİZASYON WRAP KAĞIDI 25 (±5) X 55 (±5)CM (Model/Catalog Number: 30100003994) is a medical device manufactured by BAYTEKS TEKNİK TEKSTİL SAN. VE TİC. A.Ş.. This product is indexed under FDA Product Code / Category Classification T0210 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 30100003994
- Product Code / EMDN
- T0210
- Device Name
- CERRAHİ ÖRTÜ
- Database Sync Date
- 2026-08-09 16:48:55
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of STERİLİZASYON WRAP KAĞIDI 25 (±5) X 55 (±5)CM?
The registered manufacturer of record for STERİLİZASYON WRAP KAĞIDI 25 (±5) X 55 (±5)CM is BAYTEKS TEKNİK TEKSTİL SAN. VE TİC. A.Ş..
What is the Primary UDI-DI identifier for STERİLİZASYON WRAP KAĞIDI 25 (±5) X 55 (±5)CM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08681744105071.
What classification code is assigned to this device?
This device is registered under product classification code T0210.
Similar Classification Devices (T0210)
Other Devices by BAYTEKS TEKNİK TEKSTİL SAN. VE TİC. A.Ş.
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