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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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syngo.CT PP_IIa_App_ERLN H 127 — 38 UDI-DI variants, MDR

MD Atlas
Siemens Healthcare GmbH

Data from EUDAMED, last updated May 23, 2026

syngo.CT PP_IIa_App_ERLN H 127

0405686900118UT

38 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: Siemens Healthcare GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 0405686900118UT
Device name: syngo.CT PP_IIa_App_ERLN H 127
Device model: syngo.CT PP_IIa_App_ERLN H 127
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: May 12, 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

38 UDI-DI variants

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Applied filters

basicUdiUlid01KRE48WC4386C9JK7ZPHY0TJ0

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

No registered UDI-DI variants for this device family.