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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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Erigo — 4 UDI-DI variants, MDR (Hocoma AG)

MD Atlas
Hocoma AG

Data from EUDAMED, last updated May 23, 2026

Erigo

764017466ERV9

4 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

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 764017466ERV9
Device name: Erigo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 28, 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

4 UDI-DI variants

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Applied filters

basicUdiUlid01K18ND5F27NJM2JDW3RJDBTTD

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

2956407640174660032
2967207640174660056
2956507640174660049
2967307629999033894