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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Einmalinstrumente Magillzangen, unsteril — 2 UDI-DI variants, MDR

MD Atlas
Fuhrmann GmbH

Data from EUDAMED, last updated May 23, 2026

Einmalinstrumente Magillzangen, unsteril

40548580251I1101J5

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Fuhrmann GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40548580251I1101J5
Device name: Einmalinstrumente Magillzangen, unsteril
Device model: Einmalinstrumente Magillzangen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 4, 2025

Manufacturer & authorised representative

Manufacturer

Name: Fuhrmann GmbH
SRN: DE-MF-000006652
Country: Germany
Email: info@fuhrmann.de

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K97EDRJDCQ5GRXG48B23394F

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Single-use Magill Forceps, large, 25 cm, non-sterile04054858345864
Single-use Magill Forceps, small, 17 cm, non-sterile04054858345871