GUDIDData
eudamed_udi Primary ID: 08699721130039

CANSINPLAST ŞEFFAF FLASTER (UDI 08699721130039)

Manufactured by CANSIN SAĞLIK GEREÇLERİ SANAYİ VE TİCARET ANONİM ŞİRKETİ

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CANSINPLAST ŞEFFAF FLASTER - Primary ID 08699721130039

Device Regulatory Overview

The CANSINPLAST ŞEFFAF FLASTER (Model/Catalog Number: 130TL) is a medical device manufactured by CANSIN SAĞLIK GEREÇLERİ SANAYİ VE TİCARET ANONİM ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification M050101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
130TL
Product Code / EMDN
M050101
Device Name
CANSINPLAST HİPOALERJİK FLASTER
Database Sync Date
2026-08-09 16:29:31

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 CANSINPLAST ŞEFFAF FLASTER?

The registered manufacturer of record for CANSINPLAST ŞEFFAF FLASTER is CANSIN SAĞLIK GEREÇLERİ SANAYİ VE TİCARET ANONİM ŞİRKETİ.

What is the Primary UDI-DI identifier for CANSINPLAST ŞEFFAF FLASTER?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08699721130039.

What classification code is assigned to this device?

This device is registered under product classification code M050101.

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