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Organization name
UDI-DI code
Reference / catalog number

1090 — Class IIa MDR by axion GmbH

MD Atlas
axion GmbH

EUDAMED last updated this device on May 15, 2026

1090

426028018TENSEMSJM

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: axion GmbH
UDI-DI code: 04260280185699
Reference / catalog number: 1090

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Manufacturer information

Organization name: axion GmbH
SRN: DE-MF-000006487
Manufacturer status: Active

Critical warnings

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

CW010
Vor der Anwendung Gebrauchsanweisung sorgfältig lesen

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Oct 1, 2024	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260280185699
Basic UDI-DI: 426028018TENSEMSJM
Reference / catalog number: 1090
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)

Z120601ELECTROTHERAPY EQUIPMENT (INCLUDED TENS)

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

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Certificates

Certificate health across this manufacturer's portfolio.

C563995Issued
Quality management systemNotified body: 2460Expiry: Jul 12, 2029