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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

00065140-1/10101554 — Class I MDR by Nordic Sense A/S

MD Atlas
Nordic Sense A/S

EUDAMED last updated this device on Feb 5, 2026

00065140-1/10101554

5707761NordicSenseG1VD

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Nordic Sense A/S
UDI-DI code: 05707761000120
Reference / catalog number: 00065140-1/10101554

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Manufacturer information

Organization name: Nordic Sense A/S
SRN: DK-MF-000042394
Manufacturer status: Active

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: 05707761000120
Basic UDI-DI: 5707761NordicSenseG1VD
Reference / catalog number: 00065140-1/10101554
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: Eksplorationsgel
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 150 MU03

EMDN nomenclature code(s)

Z1399NON-SPECIFIC CONSUMABLES FOR DIAGNOSTIC INSTRUMENTS - OTHER

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

Ceduren Exploration gel5707761NordicSenseG1VDOn 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.