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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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SeeLuma, Heidelberg OPERA — 3 UDI-DI variants, MDR

MD Atlas
Munich Surgical Imaging GmbH

Data from EUDAMED, last updated May 23, 2026

SeeLuma, Heidelberg OPERA

4064434SeeLumaRZ

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Munich Surgical Imaging GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4064434SeeLumaRZ
Device name: SeeLuma, Heidelberg OPERA
Device model: V10710-01, V12200-01, V12404-01
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: Munich Surgical Imaging GmbH
SRN: DE-MF-000009644
Country: Germany
Email: info@munichimaging.de

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HAM7S3E62SFWBM9JE0ZRYV7X

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

Heidelberg OPERA04064434000216
V10710-0104064434000049
V12200-0104064434000131