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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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KMINA and PEPE Rollators — 18 UDI-DI variants, MDR

MD Atlas
Improving Mobility Development SL

Data from EUDAMED, last updated May 23, 2026

KMINA and PEPE Rollators

436584K10000BDF

18 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: Improving Mobility Development SL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 436584K10000BDF
Device name: KMINA and PEPE Rollators
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 1, 2025

Manufacturer & authorised representative

Manufacturer

Name: Improving Mobility Development SL
SRN: ES-MF-000010985
Country: Spain
Email: admin@kmina.com
Phone: +34 626 34 02 07

Variants by status

UDI-DI variants

18 UDI-DI variants

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Applied filters

basicUdiUlid01JQRGKE7TR9K46CAG28AMHDHK

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

K1001008436584360056
K1000908436584360049
K1006308436584363422
K1001608436584360575
K1001508436584360070
K1001208436584360551
K1001108436584360063
K1001408436584360568
K1001308436584360346
K1001708436584360988
K1005508436584361725
K1004708436584361152
K1006008436584362500
P1000308436584360353
P1001208436584361565
P1003208436584364542
P1002208436584363439
P1000708436584360995