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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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Organization name
UDI-DI code
Reference / catalog number

RayStation RayCommand v2025 SPC1 — Class IIb MDR

MD Atlas
RAYSEARCH LABORATORIES AB (PUBL)

EUDAMED last updated this device on May 11, 2026

RayStation RayCommand v2025 SPC1

73500020105HG

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: RAYSEARCH LABORATORIES AB (PUBL)
UDI-DI code: 07350002010921
Reference / catalog number: 17.1

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View device family (Basic UDI)

Manufacturer information

Organization name: RAYSEARCH LABORATORIES AB (PUBL)
SRN: SE-MF-000001908
Manufacturer status: Active

Related devices

RayCare v202573500020106HJOn the market RayCare v2025 SP173500020106HJOn the market RayStation RayCommand v2025 SPC273500020105HGOn the market RayStation v2025 SP173500020105HGOn the market RayStation v2025 SP273500020105HGOn the market

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Austria; available across 1 country total.

Country	On market since	Until
AustriaPrimary placement	Oct 22, 2025	Still on market

Device identification

Trade name: RayStation RayCommand v2025 SPC1
UDI-DI code: 07350002010921
Basic UDI-DI: 73500020105HG
Reference / catalog number: 17.1
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)07350002010921

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z11019082VARIOUS RADIOTHERAPY AND RADIOSURGERY INSTRUMENTS - SOFTWARE ACCESSORIES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.