GUDIDData
eudamed_udi Primary ID: 04054858000688

Mullkompressen-Set, steril à 10 Stück, 10 x 13 cm, 16-fach, Röntgenkontrast, 17-fädig, steril (UDI 04054858000688)

Manufactured by Fuhrmann GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Mullkompressen-Set, steril à 10 Stück, 10 x 13 cm, 16-fach, Röntgenkontrast, 17-fädig, steril - Primary ID 04054858000688

Device Regulatory Overview

The Mullkompressen-Set, steril à 10 Stück, 10 x 13 cm, 16-fach, Röntgenkontrast, 17-fädig, steril (Model/Catalog Number: 31131) is a medical device manufactured by Fuhrmann GmbH. This product is indexed under FDA Product Code / Category Classification M0201050201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
31131
Product Code / EMDN
M0201050201
Device Name
Mullkompressen mit Röntgenkontrast, dampfsteril
Database Sync Date
2026-08-09 16:28:44

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 Mullkompressen-Set, steril à 10 Stück, 10 x 13 cm, 16-fach, Röntgenkontrast, 17-fädig, steril?

The registered manufacturer of record for Mullkompressen-Set, steril à 10 Stück, 10 x 13 cm, 16-fach, Röntgenkontrast, 17-fädig, steril is Fuhrmann GmbH.

What is the Primary UDI-DI identifier for Mullkompressen-Set, steril à 10 Stück, 10 x 13 cm, 16-fach, Röntgenkontrast, 17-fädig, steril?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04054858000688.

What classification code is assigned to this device?

This device is registered under product classification code M0201050201.

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