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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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Exploration and Ultrasound Gel — 2 UDI-DI variants, MDR

MD Atlas
Nordic Sense A/S

Data from EUDAMED, last updated May 23, 2026

Exploration and Ultrasound Gel

5707761NordicSenseG1VD

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Nordic Sense A/S

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5707761NordicSenseG1VD
Device name: Exploration and Ultrasound Gel
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 24, 2024

Manufacturer & authorised representative

Manufacturer

Name: Nordic Sense A/S
SRN: DK-MF-000042394
Country: Denmark
Email: info@nordicsense.dk

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01J150D565PB18J9W21T9Y8DSJ

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

00065140-1/1010155405707761000120
Ceduren Exploration gel05707761000007