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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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RayStation — 4 UDI-DI variants, MDR (RAYSEARCH LABORATORIES AB (PUBL))

MD Atlas
RAYSEARCH LABORATORIES AB (PUBL)

Data from EUDAMED, last updated May 31, 2026

RayStation

73500020105HG

4 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: RAYSEARCH LABORATORIES AB (PUBL)

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 73500020105HG
Device name: RayStation
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: Apr 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: RAYSEARCH LABORATORIES AB (PUBL)
SRN: SE-MF-000001908
Country: Sweden
Email: quality@raysearchlabs.com
Phone: +46 8 510 530 00

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KQCWA02WMHAK0R76B5K1TMYZ

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

RayStation RayCommand v2025 SPC107350002010921
RayStation RayCommand v2025 SPC207350002011058
RayStation v2025 SP107350002010945
RayStation v2025 SP207350002010969