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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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WÖLINO — 1 UDI-DI variant, MDD (Rehasense Sp. z o.o.)

MD Atlas
Rehasense Sp. z o.o.

Data from EUDAMED, last updated May 30, 2026

WÖLINO

B-05907467836027

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class I

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: Rehasense Sp. z o.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: B-05907467836027
Device name: WÖLINO
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: May 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: Rehasense Sp. z o.o.
SRN: PL-MF-000004772
Country: Poland
Email: arkadiusz.fijalkowski@rehasense.com
Phone: +48 698 494 335

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01JWEDT17NRFRZT5EZ2V6956M5

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

CRBKL600WZ05907467836027