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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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Psoriasis Gel — 1 UDI-DI variant, MDR (Cannordic A/S )

MD Atlas
Cannordic A/S

Data from EUDAMED, last updated May 31, 2026

Psoriasis Gel

574400013MDPSOG20MU

1 UDI-DI variant

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

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

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Device characteristics

No device characteristics flagged

Clinical investigations

Investigation number: 411033
Registered: No
Countries: India

Identity & classification

Basic UDI-DI: 574400013MDPSOG20MU
Device name: Psoriasis Gel
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 29, 2024

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

basicUdiUlid01JBCARFGP1HVAJXMXTMGHDGR5

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 Psoriasis Gel05744000130378