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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/Acculan saw blade (SU) — 40 UDI-DI variants, MDR (Aesculap AG)

MD Atlas
Aesculap AG

Data from EUDAMED, last updated May 23, 2026

ELAN 4/Acculan saw blade (SU)

40392390000014622G

40 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: 40392390000014622G
Device name: ELAN 4/Acculan saw blade (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

40 UDI-DI variants

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Applied filters

basicUdiUlid01KAB2BAZHQPD14TDGP2QS93ST

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 404046955199273
ELAN 404046955157648
ELAN 404046955157624
ELAN 404046955157617
ELAN 404046955157679
ELAN 404046955157570
ELAN 404046955157631
ELAN 404046955157662
ELAN 404046955157600
ELAN 404046955157587
ELAN 404046955157686
ELAN 404046955157594
ELAN 404046955199297
ELAN 404046955199280
ELAN 404046955157655

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