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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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ELAN 4 rotating instrument (SU) — 190 UDI-DI variants, MDR

MD Atlas
Aesculap AG

Data from EUDAMED, last updated May 23, 2026

ELAN 4 rotating instrument (SU)

40392390000014582R

190 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: Aesculap AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40392390000014582R
Device name: ELAN 4 rotating instrument (SU)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 18, 2025

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

190 UDI-DI variants

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Applied filters

basicUdiUlid01KAB42EHEH5ESCBR66SPDTCWA

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

ELAN 404046955152001
ELAN 404046955152988
ELAN 404046955152445
ELAN 404046955153503
ELAN 404046955153459
ELAN 404046955153176
ELAN 404046955151509
ELAN 404046955153572
ELAN 404046955152964
ELAN 404046955151929
ELAN 404046955151943
ELAN 404046955152612
ELAN 404046955152605
ELAN 404046955152995
ELAN 404046955152827

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