GUDIDData
eudamed_udi Primary ID: 05900516895518

ABSORBA (UDI 05900516895518)

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 ABSORBA - Primary ID 05900516895518

Device Regulatory Overview

The ABSORBA (Model/Catalog Number: MA-152-RMWY-008) is a medical device manufactured by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA. This product is indexed under FDA Product Code / Category Classification M040301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
MA-152-RMWY-008
Product Code / EMDN
M040301
Device Name
DRESSING MATERIALS - NON-INVASIVE STERILE
Database Sync Date
2026-08-09 16:59:00

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 ABSORBA?

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

What is the Primary UDI-DI identifier for ABSORBA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05900516895518.

What classification code is assigned to this device?

This device is registered under product classification code M040301.

Similar Classification Devices (M040301)

Other Devices by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA

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