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Organization name
UDI-DI code
Reference / catalog number

RAY-TWO+ — Class IIa MDR by eLEDricity bv

MD Atlas
eLEDricity bv

EUDAMED last updated this device on Apr 23, 2026

RAY-TWO+

5430003736RAY2S9

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: eLEDricity bv
UDI-DI code: 05430003736043
Reference / catalog number: ZA-08-Z-001

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Manufacturer information

Organization name: eLEDricity bv
SRN: BE-MF-000022127
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW999
UV-C emitted inside this product contains per IEC 62471 a UV-C LED source of Risk Group 3: Avoid eye and skin exposure to unshielded product.

Market distribution

Primary placement in Belgium; available across 1 country total.

Country	On market since	Until
BelgiumPrimary placement	Jan 31, 2026	Still on market

Device identification

Trade name: RAY-TWO+
UDI-DI code: 05430003736043
Basic UDI-DI: 5430003736RAY2S9
Reference / catalog number: ZA-08-Z-001
Issuing entity: GS1

Classification

Risk category: Class IIa
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.

EMDN nomenclature code(s)

Z12011301CLEANING AND DISINFECTION EQUIPMENT

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

This device is not currently linked to any other device.

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.