Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Arm Light Exoskeleton Rehab Station — 1 UDI-DI variant, MDR

MD Atlas
Wearable Robotics s.r.l.

Data from EUDAMED, last updated May 31, 2026

Arm Light Exoskeleton Rehab Station

805257513000BA

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Wearable Robotics s.r.l.

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Active device

Clinical investigations

Registered: No

Registered: No

Legacy certificates

Certificate number: MDR 00153-A
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: KIWA CERMET ITALIA S.P.A. (0476)
Validity: Sep 22, 2025 → Sep 21, 2030

Identity & classification

Basic UDI-DI: 805257513000BA
Device name: Arm Light Exoskeleton Rehab Station
Device model: ALEx-RS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Dec 9, 2025

Manufacturer & authorised representative

Manufacturer

Name: Wearable Robotics s.r.l.
SRN: IT-MF-000035444
Country: Italy
Email: info@wearable-robotics.com
Phone: +39 0505493239

Variants by status

UDI-DI variants

1 UDI-DI variant

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KC1E5KE504GDJJ94NG98JG1C

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

ALEx-RS08052575130004