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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

LICENSE — Class I MDR by Medodan Consulting ApS

MD Atlas
Medodan Consulting ApS

EUDAMED last updated this device on Oct 20, 2025

LICENSE

5745001004_LicenseW4

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Medodan Consulting ApS
UDI-DI code: 05745001004002
Reference / catalog number: LICENSE

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View device family (Basic UDI)

Manufacturer information

Organization name: Medodan Consulting ApS
SRN: DK-MF-000049322
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Denmark; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 05745001004002
Basic UDI-DI: 5745001004_LicenseW4
Reference / catalog number: LICENSE
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: The intended purpose of the system is that it shall measure and store real-time weight values for urine, IV, bladder flush, drain and cups of liquid for oral intake. The measurements are collected and saved for further analysis. The data shall be made available for review by the clinical or research personnel via a graphical user interface on a portable device, such as a tablet or laptop. The License III system is not intended for making diagnosis or decisions about specific patients
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05745001004002

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

V030206UROLOGY MEASUREMENT DEVICES 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

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Related devices

LICENSE5745001004_LicenseW4On 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.