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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

deepcOS AIDA — Class IIa MDR by deepc GmbH

MD Atlas
deepc GmbH

EUDAMED last updated this device on Nov 25, 2024

deepcOS AIDA

4260683024007UW

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: deepc GmbH
UDI-DI code: 04260683024007
Reference / catalog number: deepcOS AIDA

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Manufacturer information

Organization name: deepc GmbH
SRN: DE-MF-000006984
Manufacturer status: Active

Critical warnings

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

CW011
Images displayed might be compressed. Use for informational purposes only.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jan 1, 2025	Mar 31, 2025

Device identification

Trade name: not provided
UDI-DI code: 04260683024007
Basic UDI-DI: 4260683024007UW
Reference / catalog number: deepcOS AIDA
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: deepcOS AIDA (v2.1) is a patient data management software with a DICOM viewer.
Additional information URL: https://www.deepc.ai/instructions-for-use
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z11039082VARIOUS RADIODIAGNOSTIC AND INTERVENTIONAL 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

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.