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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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Patient Reference Clamp Spine & Trauma — 3 UDI-DI variants, MDR

MD Atlas
Brainlab SE

Data from EUDAMED, last updated May 23, 2026

Patient Reference Clamp Spine & Trauma

4056481SpineRefClampET

3 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: Brainlab SE

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4056481SpineRefClampET
Device name: Patient Reference Clamp Spine & Trauma
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 22, 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

3 UDI-DI variants

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Applied filters

basicUdiUlid01JVW220K44S7AZ0TFRW6A1QY3

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

5582604056481146054
5582504056481145446
5582404056481145439