GUDIDData
eudamed_udi Primary ID: 05900516224776

MATODRAPE (UDI 05900516224776)

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 MATODRAPE - Primary ID 05900516224776

Device Regulatory Overview

The MATODRAPE (Model/Catalog Number: MB-135-ZOL2-008) is a medical device manufactured by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA. This product is indexed under FDA Product Code / Category Classification T020102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
MB-135-ZOL2-008
Product Code / EMDN
T020102
Device Name
DISPOSABLE DRAPES, SETS, COVERS AND ACCESSORIES STERILE
Database Sync Date
2026-08-09 16:29:19

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 MATODRAPE?

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

What is the Primary UDI-DI identifier for MATODRAPE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05900516224776.

What classification code is assigned to this device?

This device is registered under product classification code T020102.

Similar Classification Devices (T020102)

Other Devices by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA

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