GUDIDData
eudamed_udi Primary ID: 08681049534743

Disposet (UDI 08681049534743)

Manufactured by DİSPOSET TIBBİ ÜRÜNLER SANAYİ VE TİCARET ANONİM ŞİRKETİ

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Disposet - Primary ID 08681049534743

Device Regulatory Overview

The Disposet (Model/Catalog Number: DS-PL200MM) is a medical device manufactured by DİSPOSET TIBBİ ÜRÜNLER SANAYİ VE TİCARET ANONİM ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification A03020102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
DS-PL200MM
Product Code / EMDN
A03020102
Device Name
Pressure Line
Database Sync Date
2026-08-09 16:28:50

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 Disposet?

The registered manufacturer of record for Disposet is DİSPOSET TIBBİ ÜRÜNLER SANAYİ VE TİCARET ANONİM ŞİRKETİ.

What is the Primary UDI-DI identifier for Disposet?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08681049534743.

What classification code is assigned to this device?

This device is registered under product classification code A03020102.

Similar Classification Devices (A03020102)

Other Devices by DİSPOSET TIBBİ ÜRÜNLER SANAYİ VE TİCARET ANONİM ŞİRKETİ

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