GUDIDData
eudamed_udi Primary ID: 08683608039973

Safecheck Tyvek® Sterilization Reel (TY40100) (UDI 08683608039973)

Manufactured by Medster Tıbbi Cihaz ve Sağlık Hizmetleri Ltd. Şti.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Safecheck Tyvek® Sterilization Reel (TY40100) - Primary ID 08683608039973

Device Regulatory Overview

The Safecheck Tyvek® Sterilization Reel (TY40100) (Model/Catalog Number: TY40100) is a medical device manufactured by Medster Tıbbi Cihaz ve Sağlık Hizmetleri Ltd. Şti.. This product is indexed under FDA Product Code / Category Classification S01020201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
TY40100
Product Code / EMDN
S01020201
Device Name
SafeCheck Sterilization Reels and Pouches
Database Sync Date
2026-08-09 16:59:30

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 Safecheck Tyvek® Sterilization Reel (TY40100)?

The registered manufacturer of record for Safecheck Tyvek® Sterilization Reel (TY40100) is Medster Tıbbi Cihaz ve Sağlık Hizmetleri Ltd. Şti..

What is the Primary UDI-DI identifier for Safecheck Tyvek® Sterilization Reel (TY40100)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08683608039973.

What classification code is assigned to this device?

This device is registered under product classification code S01020201.

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