GUDIDData
eudamed_udi Primary ID: 05900516861339

MATOPAT UNIVERSAL (UDI 05900516861339)

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 MATOPAT UNIVERSAL - Primary ID 05900516861339

Device Regulatory Overview

The MATOPAT UNIVERSAL (Model/Catalog Number: MA-123-UN50-034) is a medical device manufactured by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA. This product is indexed under FDA Product Code / Category Classification M0304010102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
MA-123-UN50-034
Product Code / EMDN
M0304010102
Device Name
BANDAGES NON STERILE
Database Sync Date
2026-08-09 16:29:40

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 MATOPAT UNIVERSAL?

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

What is the Primary UDI-DI identifier for MATOPAT UNIVERSAL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05900516861339.

What classification code is assigned to this device?

This device is registered under product classification code M0304010102.

Similar Classification Devices (M0304010102)

Other Devices by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA

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