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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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RegenET/CT — 2 UDI-DI variants, MDR (Regen Lab SA)

MD Atlas
Regen Lab SA

Data from EUDAMED, last updated May 23, 2026

RegenET/CT

764013898REGENETCTT2

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: Regen Lab SA

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 764013898REGENETCTT2
Device name: RegenET/CT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 7, 2025

Manufacturer & authorised representative

Manufacturer

Name: Regen Lab SA
SRN: CH-MF-000032231
Country: Switzerland
Email: ddiermen@regenlab.com
Phone: +41 21 864 01 11

Authorised representative

Name: RegenLab France
SRN: FR-AR-000011953
Country: France
Phone: +33 (0)7 62 33 22 24

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K6YQVGWY4GD6XYZJ30RAGTEB

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-CT-307640138980084
R-ET-307640138981364