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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

DR. INFO — Class I MDR by Synduct GmbH

MD Atlas
Synduct GmbH

EUDAMED last updated this device on Mar 20, 2026

DR. INFO

426258275DRINFOFF

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Synduct GmbH
UDI-DI code: 04262582750018
Reference / catalog number: DRINFO-v2

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Manufacturer information

Organization name: Synduct GmbH
SRN: DE-MF-000052647
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: DR. INFO
UDI-DI code: 04262582750018
Basic UDI-DI: 426258275DRINFOFF
Reference / catalog number: DRINFO-v2
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: Informational and educational software platform (SaMD) for qualified healthcare professionals. Retrieves and displays drug information, interaction data, and clinical guidelines from verified authoritative medical sources.
Additional information URL: https://drinfo.ai/
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.