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.

LokomatPro — 9 UDI-DI variants, MDR (Hocoma AG)

MD Atlas
Hocoma AG

Data from EUDAMED, last updated May 23, 2026

LokomatPro

764017466L6U8

9 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: Hocoma AG

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

Identity & classification

Basic UDI-DI: 764017466L6U8
Device name: LokomatPro
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: Hocoma AG
SRN: CH-MF-000014672
Country: Switzerland
Email: info.hocoma@dih.com

Authorised representative

Name: Emergo Europe B.V.
SRN: NL-AR-000000116
Country: Netherlands
Phone: +31 70 345 8570

Variants by status

UDI-DI variants

9 UDI-DI variants

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

basicUdiUlid01K1B7ATWTC68SZPHETD46YV7R

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

6305607640174660445
6305907640174660476
6305307640174660414
6305207640174660407
6305407640174660421
6305507640174660438
6305807640174660469
6305707640174660452
6306007640174660483