GUDIDData
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eudamed_udi Primary ID: 04054858024981

Schlinggazetupfer, 15 x 15 cm, VM 20, unsteril (UDI 04054858024981)

Manufactured by Fuhrmann GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Schlinggazetupfer, 15 x 15 cm, VM 20, unsteril - Primary ID 04054858024981

Device Regulatory Overview

The Schlinggazetupfer, 15 x 15 cm, VM 20, unsteril (Model/Catalog Number: 40709) is a medical device manufactured by Fuhrmann GmbH. This product is indexed under FDA Product Code / Category Classification M0201020102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
40709
Product Code / EMDN
M0201020102
Device Name
Schlinggazetupfer ohne Röntgenkontrast, unsteril
Database Sync Date
2026-08-09 16:30:03

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, 15 x 15 cm, VM 20, unsteril?

The registered manufacturer of record for Schlinggazetupfer, 15 x 15 cm, VM 20, unsteril is Fuhrmann GmbH.

What is the Primary UDI-DI identifier for Schlinggazetupfer, 15 x 15 cm, VM 20, unsteril?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04054858024981.

What classification code is assigned to this device?

This device is registered under product classification code M0201020102.

Similar Classification Devices (M0201020102)

Other Devices by Fuhrmann GmbH

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