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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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WÓZEK INWALIDZKI CRUISER ACTIVE… — 8 UDI-DI variants, MDR

MD Atlas
REHA FUND Sp. z o.o.

Data from EUDAMED, last updated May 31, 2026

WÓZEK INWALIDZKI CRUISER ACTIVE (CZARNY)

59039407RF3Z9

8 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: REHA FUND Sp. z o.o.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 59039407RF3Z9
Device name: WÓZEK INWALIDZKI CRUISER ACTIVE (CZARNY)
Device model: RF-3
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: REHA FUND Sp. z o.o.
SRN: PL-MF-000047481
Country: Poland
Email: jakosc@rehafund.pl

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KPQRTA4CCFK53JT0W2JAWMG6

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

WHEELCHAIR CRUISER ACTIVE (BLACK)05903940701516
WHEELCHAIR CRUISER ACTIVE (BLACK)05903940709567
WHEELCHAIR CRUISER ACTIVE (BLACK)05903940701530
WHEELCHAIR CRUISER ACTIVE (BLACK)05903940701554
WHEELCHAIR CRUISER ACTIVE (BLACK)05903940701523
WÓZEK INWALIDZKI CRUISER ACTIVE (CZARNY)05903940701547
HEELCHAIR CRUISER ACTIVE (BLACK)05903940709550
WHEELCHAIR CRUISER ACTIVE (BLACK)05903940701509