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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 Electric Wheelchairs… — 7 UDI-DI variants, MDR

MD Atlas
Improving Mobility Development SL

Data from EUDAMED, last updated May 23, 2026

KMINA and PEPE Electric Wheelchairs and Mobility Scooters

436584K1000FMZ

7 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: 436584K1000FMZ
Device name: KMINA and PEPE Electric Wheelchairs and Mobility Scooters
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 18, 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

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K2Y63DTT00JS6GVQSH4J9G79

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

P1004408436584364740
P1004308436584364733
P1004208436584364726
K1007308436584364757
K1007408436584364788
K1007608436584364801
K1007508436584364795