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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

ST_AX_0000 REV.0 — Class I MDR by ATENA LUX S.R.L.

MD Atlas
ATENA LUX S.R.L.

EUDAMED last updated this device on May 14, 2026

ST_AX_0000 REV.0

8059692660000CLIV3

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ATENA LUX S.R.L.
UDI-DI code: 08059692660001
Reference / catalog number: ST_AX_0000 REV.0

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View device family (Basic UDI)

Manufacturer information

Organization name: ATENA LUX S.R.L.
SRN: IT-MF-000016765
Manufacturer status: Active

Related devices

4251-----8059692660000CLIV3On the market 4254-----8059692660000CLIV3On the market ST_AR_0000 REV.X8059692660000CLIV3On the market ST_AR_0000 REV.X8059692660000CLIV3On the market ST_AR_0000 REV.X805969266000CLIIA8LOn the market

Certificates

Certificate health across this manufacturer's portfolio.

015-00-00-MDRIssued
Quality management systemNotified body: 0426Expiry: Mar 20, 2028

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW273
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08059692660001
Basic UDI-DI: 8059692660000CLIV3
Reference / catalog number: ST_AX_0000 REV.0
Issuing entity: GS1

Classification

Risk category: Class I
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

EMDN nomenclature code(s)

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

Z129017BED HEAD UNITS

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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