- Role
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- Date of registration
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EUDAMED last updated this device on Oct 14, 2025
366039600099BGPROTECTION CONFORT QUINTUS VARUS EPITACT / COMFORT BESCHERMER QUINTUS VARUS EPITACT / KOMFORTSCHUTZES QUINTUS VARUS EPITACT is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Millet Innovation. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
FR-MF-000004611(01)03660396019887
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
3 warnings recorded — scroll inside the panel to see all entries.
For people with arteritis, phlebitis, diabetes, lower limb neuropathy or allergy to any of the components: ask a health professional for advice and then monitor your foot during use.
Do not use on damaged skin
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in France; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | — | Still on market |
| Belgium | — | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
03660396019887Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
366039600099BGQV013BEUDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Y061203ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS)Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →No certificate specifically references this device's Basic UDI-DI.
366039600002A7On the marketPROTECTION CONFORT QUINTUS VARUS EPITACT / COMFORT BESCHERMER QUINTUS VARUS EPITACT / KOMFORTSCHUTZES QUINTUS VARUS EPITACT366039600099BGOn the marketPROTECTION CONFORT QUINTUS VARUS EPITACT / COMFORT BESCHERMER QUINTUS VARUS EPITACT / KOMFORTSCHUTZES QUINTUS VARUS EPITACT366039600099BGOn the marketProtection Hallux Valgus "oignon"366039600005ADOn the marketProtection Hallux Valgus "oignon"366039600005ADOn the marketProtection Hallux Valgus "oignon"366039600005ADOn the marketNo certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.