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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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Rongeur — 147 UDI-DI variants, MDR (Aesculap AG)

MD Atlas
Aesculap AG

Data from EUDAMED, last updated May 23, 2026

Rongeur

403923900000051729

147 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Aesculap AG

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 403923900000051729
Device name: Rongeur
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 8, 2025

Manufacturer & authorised representative

Manufacturer

Name: Aesculap AG
SRN: DE-MF-000005504
Country: Germany
Email: eudamed@bbraun.com

Variants by status

UDI-DI variants

147 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K71CR20HN5BV6P4XKY6CZGE1

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

Noir®04046964608193
Noir®04046964608810
Noir®04046964608667
Noir®04046964608131
Noir®04046964608247
Noir®04046964608728
Noir®04046964608803
Noir®04046964608681
Noir®04046964608896
Noir®04046964608414
Noir®04046964608209
Noir®04046964608186
Noir®04046964608162
Noir®04046964608742
Noir®04046964608933
Noir®04046964608940
Noir®04046964608926
Noir®04046964608674
Noir®04046964608506
Noir®04046964608537
Noir®04046964608117
Noir®04046964608568
Noir®04046964608179
Noir®04046964609404
Noir®04046964608773

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