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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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RAYLYTIC PROMs — 2 UDI-DI variants, MDR (RAYLYTIC Software GmbH)

MD Atlas
RAYLYTIC Software GmbH

Data from EUDAMED, last updated May 23, 2026

RAYLYTIC PROMs

4262473810002WE

2 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: RAYLYTIC Software GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4262473810002WE
Device name: RAYLYTIC PROMs
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Special device type: refdata.special-mdr-device-type.software
Version date: May 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: RAYLYTIC Software GmbH
SRN: DE-MF-000044964
Country: Germany
Email: support@raylytic.com
Phone: +49 341 656702-01

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KRZH5M86WCCFXSY3TYMY7M86

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

RAYLYTIC PROMs04262473810029
RAYLYTIC PROMs42624738100298