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EUDAMED last updated this device on May 10, 2026
326824F3429-01YGEXEOL SEPT FOAM 12X750ML is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by SODEL. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
03268240061824EXS0141Z11 packaging level registered — each level carries its own UDI-DI.
03268240061824× 1 unitBase unit13268240061821× 12 units(01)03268240061824
European Medical Device Nomenclature — the EU product classification assigned to this device.
D0902ASSOCIATED AMMONIUM SALTS FOR THE DISINFECTION OF MEDICAL DEVICES8 warnings recorded — scroll inside the panel to see all entries.
Lésions oculaires graves/irritation oculaire, catégorie 2 H319 [FR] - Serious eye damage/eye irritation, Category 2 H319 [EN]
Provoque une sévère irritation des yeux. [FR] - Causes serious eye irritation. [EN]
Porter un équipement de protection des yeux. [FR] - Wear eye protection. [EN]
EN CAS DE CONTACT AVEC LES YEUX: Enlever les lentilles de contact si la victime en porte et si elles peuvent être facilement enlevées. Continuer à rincer. [FR] - IF IN EYES: Remove contact lenses, if present and easy to do. Continue rinsing. [EN]
EN CAS DE CONTACT AVEC LES YEUX: Rincer avec précaution à l’eau pendant plusieurs minutes. [FR] - IF IN EYES: Rinse cautiously with water for several minutes. [EN]
Primary placement in France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Sep 1, 2026 | Still on market |
FR-MF-000000367The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Si l’irritation oculaire persiste: consulter un médecin. [FR] - If eye irritation persists: Get medical advice/attention. [EN]
OTHER
OTHER
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.
View in glossary →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.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
View in glossary →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 →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →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.
View in glossary →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.
Certificate health across this manufacturer's portfolio.
39301Supplemented40077Issued39947IssuedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →Notified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →Notified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →