GUDIDData
eudamed_udi Primary ID: 08681227034508

SafeCheck Tyvek® Sterilization Pouch (TYZ1535) (UDI 08681227034508)

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 Pouch (TYZ1535) - Primary ID 08681227034508

Device Regulatory Overview

The SafeCheck Tyvek® Sterilization Pouch (TYZ1535) (Model/Catalog Number: TYZ1535) is a medical device manufactured by Medster Tıbbi Cihaz ve Sağlık Hizmetleri Ltd. Şti.. This product is indexed under FDA Product Code / Category Classification S01010201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
TYZ1535
Product Code / EMDN
S01010201
Device Name
SafeCheck Sterilization Reels and Pouches
Database Sync Date
2026-08-09 16:48:34

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 Pouch (TYZ1535)?

The registered manufacturer of record for SafeCheck Tyvek® Sterilization Pouch (TYZ1535) is Medster Tıbbi Cihaz ve Sağlık Hizmetleri Ltd. Şti..

What is the Primary UDI-DI identifier for SafeCheck Tyvek® Sterilization Pouch (TYZ1535)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08681227034508.

What classification code is assigned to this device?

This device is registered under product classification code S01010201.

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