GUDIDData
eudamed_udi Primary ID: 04054858002361

Schlinggazetupfer 25 x 25 cm, Röntgenkontrast, à 10 Stück, 20-fädig, steril (UDI 04054858002361)

Manufactured by Fuhrmann GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Schlinggazetupfer 25 x 25 cm, Röntgenkontrast, à 10 Stück, 20-fädig, steril - Primary ID 04054858002361

Device Regulatory Overview

The Schlinggazetupfer 25 x 25 cm, Röntgenkontrast, à 10 Stück, 20-fädig, steril (Model/Catalog Number: 32031) is a medical device manufactured by Fuhrmann GmbH. This product is indexed under FDA Product Code / Category Classification M0201020201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
32031
Product Code / EMDN
M0201020201
Device Name
Schlinggazetupfer mit Röntgenkontrast, dampfsteril
Database Sync Date
2026-08-09 16:29:38

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 Schlinggazetupfer 25 x 25 cm, Röntgenkontrast, à 10 Stück, 20-fädig, steril?

The registered manufacturer of record for Schlinggazetupfer 25 x 25 cm, Röntgenkontrast, à 10 Stück, 20-fädig, steril is Fuhrmann GmbH.

What is the Primary UDI-DI identifier for Schlinggazetupfer 25 x 25 cm, Röntgenkontrast, à 10 Stück, 20-fädig, steril?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04054858002361.

What classification code is assigned to this device?

This device is registered under product classification code M0201020201.

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