GUDIDData
eudamed_udi Primary ID: 08681161450389

TYVEK STERILIZATION REEL 25cm*70mt (UDI 08681161450389)

Manufactured by FTM AMBALAJ MEDİKAL İTH. İHR. SAN. VE TİC.LTD. ŞTİ

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TYVEK STERILIZATION REEL 25cm*70mt - Primary ID 08681161450389

Device Regulatory Overview

The TYVEK STERILIZATION REEL 25cm*70mt (Model/Catalog Number: FTM-00-038) is a medical device manufactured by FTM AMBALAJ MEDİKAL İTH. İHR. SAN. VE TİC.LTD. ŞTİ. This product is indexed under FDA Product Code / Category Classification S01020201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
FTM-00-038
Product Code / EMDN
S01020201
Device Name
TYVEK STREILIZATION REEL
Database Sync Date
2026-08-09 16:44:57

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 STERILIZATION REEL 25cm*70mt?

The registered manufacturer of record for TYVEK STERILIZATION REEL 25cm*70mt is FTM AMBALAJ MEDİKAL İTH. İHR. SAN. VE TİC.LTD. ŞTİ.

What is the Primary UDI-DI identifier for TYVEK STERILIZATION REEL 25cm*70mt?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08681161450389.

What classification code is assigned to this device?

This device is registered under product classification code S01020201.

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