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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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Alegro Arnikate — 4 UDI-DI variants, MDR (Alegro Medical GmbH)

MD Atlas
Alegro Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Alegro Arnikate

PP00597ALGCFV00864

4 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: Alegro Medical GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: PP00597ALGCFV00864
Device name: Alegro Arnikate
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: Alegro Medical GmbH
SRN: DE-MF-000026024
Country: Germany
Email: info@alegromedical.de
Phone: +49 6841 777740

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KS2ZJ0MVDC03CGTVFEVRWK7G

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

7050604260585130684
7050504260585130677
71040 / 7110204260585132336
71041 / 7110204260585132343