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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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Pain & Arthritis Gel — 1 UDI-DI variant, MDD (Cannordic A/S )

MD Atlas
Cannordic A/S

Data from EUDAMED, last updated May 31, 2026

Pain & Arthritis Gel

B-05744000130002

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class I

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: Cannordic A/S

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: B-05744000130002
Device name: Pain & Arthritis Gel
Device model: MDARTG20
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: Feb 10, 2023

Manufacturer & authorised representative

Manufacturer

Name: Cannordic A/S
SRN: DK-MF-000003852
Country: Denmark
Email: info@cannordic.com
Phone: +45 70 70 73 37

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01GEEEM9JJ36H2BWZCNQK6ZV8Y

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

CANNASEN® Pain & Arthritis Gel05744000130002