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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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Wooden underarm crutch — 5 UDI-DI variants, MDR

MD Atlas
Michal Kačur TOPOR s. r. o.

Data from EUDAMED, last updated May 31, 2026

Wooden underarm crutch

8588004023BRLD2

5 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: Michal Kačur TOPOR s. r. o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8588004023BRLD2
Device name: Wooden underarm crutch
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Michal Kačur TOPOR s. r. o.
SRN: SK-MF-000053158
Country: Slovakia
Email: kacur@kacur.sk

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KNKEDGDV2M9RMZHNPBD9EKMJ

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

K2034808588004023031
K2034708588004023079
K9236308588004023024
K2034608588004023017
K9236208588004023062