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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 Alginate — 40 UDI-DI variants, MDR (Alegro Medical GmbH)

MD Atlas
Alegro Medical GmbH

Data from EUDAMED, last updated May 23, 2026

ALEGRO Alginate

PP00597ALGCFV00142

40 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: PP00597ALGCFV00142
Device name: ALEGRO Alginate
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 24, 2022

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

40 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GJFEVBSBTS1J3GG1NP5ZKRRM

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

7106404260585132121
7106304260585132138
7106104260585132152
71021 / 6002704260585132268
71026 / 6002104260585132213
71025 / 6002204260585132220
71023 / 6002304260585132237
71022 / 6002504260585132251
71024 / 6002404260585132244
71111 / 6104204260585132282
7111404260585132312
71113 / 6104604260585132305
71110 / 6104104260585132275
63033111257315558
63036111257316124

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