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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

2.6 — Class I MDR by Humanomed IT Solutions…

MD Atlas
Humanomed IT Solutions GmbH

EUDAMED last updated this device on May 21, 2026

2.6

9120135420065X

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Humanomed IT Solutions GmbH
UDI-DI code: 09120135420069
Reference / catalog number: 2.6

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Manufacturer information

Organization name: Humanomed IT Solutions GmbH
SRN: AT-MF-000041701
Manufacturer status: Active

Market distribution

Primary placement in Austria; available across 2 countries total.

Country	On market since	Until
AustriaPrimary placement	May 26, 2026	May 31, 2028
Germany	May 26, 2026	May 31, 2028

Device identification

Trade name: not provided
UDI-DI code: 09120135420069
Basic UDI-DI: 9120135420065X
Reference / catalog number: 2.6
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: Software identification
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

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

2.59120135420055VOn the market App 2.59120135420045TOn the market App 2.69120135420075ZOn the market

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.