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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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ABLE Exoskeleton — 2 UDI-DI variants, MDR (ABLE Human Motion)

MD Atlas
ABLE Human Motion

Data from EUDAMED, last updated May 23, 2026

ABLE Exoskeleton

8437025514A1EF

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: ABLE Human Motion

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Device characteristics

Active device

Clinical investigations

Registered: No

Registered: No

Registered: No

Identity & classification

Basic UDI-DI: 8437025514A1EF
Device name: ABLE Exoskeleton
Device model: A1
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 2, 2024

Manufacturer & authorised representative

Manufacturer

Name: ABLE Human Motion
SRN: ES-MF-000037009
Country: Spain
Email: hello@ablehumanmotion.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HTFGX8FZ23D7N3AW2V5WJST8

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

ABLE Exoskeleton08437025514007
A1-RC08437025514045