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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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FOOTWEAR — 30 UDI-DI variants, MDR (CALZAMEDI, S.L.)

MD Atlas
CALZAMEDI, S.L.

Data from EUDAMED, last updated May 23, 2026

FOOTWEAR

84356621FOOTWEARE2

30 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: CALZAMEDI, S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84356621FOOTWEARE2
Device name: FOOTWEAR
Device model: FOOTWEAR
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 3, 2024

Manufacturer & authorised representative

Manufacturer

Name: CALZAMEDI, S.L.
SRN: ES-MF-000006249
Country: Spain
Email: info@calzamedi.com
Phone: +34 965817960

Variants by status

UDI-DI variants

30 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JE5TETASD4FCWTFY795GNMHK

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

0006-4308435662100263
0006-4408435662100270
0006-4508435662100287
0006-4608435662100294
0006-4708435662100300

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