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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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Alignment Software Cranial — 2 UDI-DI variants, MDR (Brainlab SE)

MD Atlas
Brainlab SE

Data from EUDAMED, last updated May 23, 2026

Alignment Software Cranial

4056481AlignmentCranialBM

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Brainlab SE

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 4056481AlignmentCranialBM
Device name: Alignment Software Cranial
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: Jul 1, 2025

Manufacturer & authorised representative

Manufacturer

Name: Brainlab SE
SRN: DE-MF-000006183
Country: Germany
Email: regulatory.affairs@brainlab.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JZ2GZRKEEDH31WTHS33939P2

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

0405648114448704056481144487
0405648114631304056481146313