GUDIDData
eudamed_udi Primary ID: 05900516235000

MATOSET (UDI 05900516235000)

Manufactured by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MATOSET - Primary ID 05900516235000

Device Regulatory Overview

The MATOSET (Model/Catalog Number: MA-991-ZESA-085) is a medical device manufactured by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA. This product is indexed under FDA Product Code / Category Classification T0202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
MA-991-ZESA-085
Product Code / EMDN
T0202
Device Name
PROCEDURE AND OPERATIVE SETS
Database Sync Date
2026-08-09 16:28:49

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 MATOSET?

The registered manufacturer of record for MATOSET is TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA.

What is the Primary UDI-DI identifier for MATOSET?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05900516235000.

What classification code is assigned to this device?

This device is registered under product classification code T0202.

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