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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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Moorpackungen — 2 UDI-DI variants, MDR (Kurland GmbH)

MD Atlas
Kurland GmbH

Data from EUDAMED, last updated May 23, 2026

Moorpackungen

4046754MoorproduktVD

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: Kurland GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4046754MoorproduktVD
Device name: Moorpackungen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 27, 2024

Manufacturer & authorised representative

Manufacturer

Name: Kurland GmbH
SRN: DE-MF-000010484
Country: Germany
Email: ranta@kurland.de

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HQN8K2Z22KRMSKP0GTE9Y9CY

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

Disposable natural Moor mud packs04046754004099
10601-0375004046754100609