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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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R-One Robotic Platform — 6 UDI-DI variants, MDR (ROBOCATH S.A.S)

MD Atlas
ROBOCATH S.A.S

Data from EUDAMED, last updated May 19, 2026

R-One Robotic Platform

3770024670RBH01P00004C

6 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: ROBOCATH S.A.S

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 3770024670RBH01P00004C
Device name: R-One Robotic Platform
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Mar 28, 2023

Manufacturer & authorised representative

Manufacturer

Name: ROBOCATH S.A.S
SRN: FR-MF-000003651
Country: France
Email: contact@robocath.com
Phone: +33 2 32 10 67 42

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GVFXK0SAN96WE18YH6EYVEH6

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

R-One Robotic Platform03770024670257
R-One Robotic Platform03770024670028
R-One Robotic Platform03770024670240
R-One Robotic Platform03770024670134
R-One Robotic Platform03770024670080
R-One Robotic Platform03770024670127