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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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MDR_18_II b_ERLN H 127_Mammo_digital — 2 UDI-DI variants, MDR

MD Atlas
Siemens Healthcare GmbH

Data from EUDAMED, last updated May 31, 2026

MDR_18_II b_ERLN H 127_Mammo_digital

0405686901979WW

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: Siemens Healthcare GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 0405686901979WW
Device name: MDR_18_II b_ERLN H 127_Mammo_digital
Device model: MDR_18_II b_ERLN H 127_Mammo_digital
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Siemens Healthcare GmbH
SRN: DE-MF-000006122
Country: Germany
Email: contact@siemens-healthineers.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KSMBTK8XTMBFQPANPE5RNJSG

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

MAMMOMAT B.brilliant04056869987187
MAMMOMAT Revelation04056869124575