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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®04046964608827
Noir®04046964608438
Noir®04046964608988
Noir®04046964608384
Noir®04046964608834
Noir®04046964608544
Noir®04046964608155
Noir®04046964608841
Noir®04046964608643
Noir®04046964608520
Noir®04046964608698
Noir®04046964608476
Noir®04046964608957
Noir®04046964608971
Noir®04046964608599
Noir®04046964608575
Noir®04046964608872
Noir®04046964608445
Noir®04046964608308
Noir®04046964608377
Noir®04046964608483
Noir®04046964608513

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