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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 saw blade (RU) — 21 UDI-DI variants, MDR (Aesculap AG)

MD Atlas
Aesculap AG

Data from EUDAMED, last updated May 23, 2026

ELAN 4 saw blade (RU)

40392390000014592T

21 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: 40392390000014592T
Device name: ELAN 4 saw blade (RU)
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

21 UDI-DI variants

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Applied filters

basicUdiUlid01KAB2BN4MAXV903A0RC70N5EB

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 404046964526954
ELAN 404046964527050
ELAN 404046964776373
ELAN 404046964527043
ELAN 404046964526978
ELAN 404046964776328
ELAN 404046964982231
ELAN 404046964526985
ELAN 404046964527005
ELAN 404046964527029
ELAN 404046955140343
ELAN 404046964526992
ELAN 404046964776366
ELAN 404046964776304
ELAN 404046964526961
ELAN 404046964527012
ELAN 404046964776359
ELAN 404046964527036
ELAN 404046964776311
ELAN 404046964776342
ELAN 404046964776335