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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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Protection QUINTUS VARUS — 9 UDI-DI variants, MDR (Millet Innovation)

MD Atlas
Millet Innovation

Data from EUDAMED, last updated May 19, 2026

Protection QUINTUS VARUS

366039600099BG

9 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Millet Innovation

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 366039600099BG
Device name: Protection QUINTUS VARUS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 27, 2024

Manufacturer & authorised representative

Manufacturer

Name: Millet Innovation
SRN: FR-MF-000004611
Country: France
Email: contact@epitact.com

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JDPEC4N96C6H8JEDQXTVEHJ4

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

QV011BE03660396019863
QV012BE03660396019870
QV013BE03660396019887
PROTECTION QUINTUS VARUS, EPITACT03660396019825
PROTECTION QUINTUS VARUS, EPITACT03660396019818
PROTECTION QUINTUS VARUS,EPITACT03660396019801
QV011IT03660396019832
QV013IT03660396019856
QV012IT03660396019849