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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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HANK Two-Wheel Mobility Scooter — 1 UDI-DI variant, MDR (Hanksconcept)

MD Atlas
Hanksconcept

Data from EUDAMED, last updated May 31, 2026

HANK Two-Wheel Mobility Scooter

8720892883610003055XV

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Hanksconcept

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8720892883610003055XV
Device name: HANK Two-Wheel Mobility Scooter
Device model: HANK TW-01
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: Hanksconcept
SRN: NL-MF-000050014
Country: Netherlands
Email: info@hanksconcept.com
Phone: +31-611510053

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KFN7P637JEVASV4ESGF8EQYE

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

HANK TW-0108720892883605