GUDIDData
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eudamed_udi Primary ID: 08030413317022

MEDIOASIS OP DRY® AIR - TAPPETINO PER PAVIMENTI IN ROTOLO MT 50 x 90 CM ASSORBENZA 2.000 ML/MQ - NON STERILE (UDI 08030413317022)

Manufactured by Mediberg S.r.l. Unipersonale

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MEDIOASIS OP DRY® AIR - TAPPETINO PER PAVIMENTI IN ROTOLO MT 50 x 90 CM ASSORBENZA 2.000 ML/MQ - NON STERILE - Primary ID 08030413317022

Device Regulatory Overview

The MEDIOASIS OP DRY® AIR - TAPPETINO PER PAVIMENTI IN ROTOLO MT 50 x 90 CM ASSORBENZA 2.000 ML/MQ - NON STERILE (Model/Catalog Number: 409010MQ2NRV) is a medical device manufactured by Mediberg S.r.l. Unipersonale. This product is indexed under FDA Product Code / Category Classification T030501 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
409010MQ2NRV
Product Code / EMDN
T030501
Device Name
TAPPETINI ASSORBENTI
Database Sync Date
2026-08-09 16:29:06

Full Regulatory Attributes

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{
    "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 MEDIOASIS OP DRY® AIR - TAPPETINO PER PAVIMENTI IN ROTOLO MT 50 x 90 CM ASSORBENZA 2.000 ML/MQ - NON STERILE?

The registered manufacturer of record for MEDIOASIS OP DRY® AIR - TAPPETINO PER PAVIMENTI IN ROTOLO MT 50 x 90 CM ASSORBENZA 2.000 ML/MQ - NON STERILE is Mediberg S.r.l. Unipersonale.

What is the Primary UDI-DI identifier for MEDIOASIS OP DRY® AIR - TAPPETINO PER PAVIMENTI IN ROTOLO MT 50 x 90 CM ASSORBENZA 2.000 ML/MQ - NON STERILE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08030413317022.

What classification code is assigned to this device?

This device is registered under product classification code T030501.

Similar Classification Devices (T030501)

Other Devices by Mediberg S.r.l. Unipersonale

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