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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

MIDA-RHEUMA-APP — Class I MDR by Midaia GmbH

MD Atlas
Midaia GmbH

EUDAMED last updated this device on May 14, 2026

MIDA-RHEUMA-APP

426073137MIDARHEUMAMDRPK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Midaia GmbH
UDI-DI code: 04260731370001
Reference / catalog number: MIDA-RHEUMA-APP

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Manufacturer information

Organization name: Midaia GmbH
SRN: DE-MF-000009779
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jun 1, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260731370001
Basic UDI-DI: 426073137MIDARHEUMAMDRPK
Reference / catalog number: MIDA-RHEUMA-APP
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.

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

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.