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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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EPIONE — 2 UDI-DI variants, MDR (Quantum Surgical SAS)

MD Atlas
Quantum Surgical SAS

Data from EUDAMED, last updated May 19, 2026

EPIONE

37603054001EPIONEUW

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: Quantum Surgical SAS

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Device characteristics

Active device

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 37603054001EPIONEUW
Device name: EPIONE
Device model: 30-0001
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Dec 21, 2021

Manufacturer & authorised representative

Manufacturer

Name: Quantum Surgical SAS
SRN: FR-MF-000000600
Country: France
Email: e.lagacherie@quantumsurgical.com
Phone: 0448194050

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FJVPDHQ1JYWNHM9MV6SHRC9R

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

30-000103760305400222
30-000103760305400307