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EUDAMED last updated this device on Sep 8, 2025
326824F3324-01WYEXEOL SURF OPTIMAL 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 Belgium. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
03268240056837EXS0038BE1 packaging level registered — each level carries its own UDI-DI.
03268240056837× 1 unitBase unit13268240056834× 12 units(01)03268240056837
European Medical Device Nomenclature — the EU product classification assigned to this device.
D0902ASSOCIATED AMMONIUM SALTS FOR THE DISINFECTION OF MEDICAL DEVICES4 warnings recorded — scroll inside the panel to see all entries.
OTHER
Ne pas mélanger à d'autres produits. Ne pas utiliser les dispositifs médicaux réutilisables en cas d'altération par le produit. [FR] - Nicht mit anderen Produkten mischen. Verwenden Sie wiederverwendbare Medizinprodukte nicht, wenn sie durch das Produkt beschädigt wurden. [DE] - Niet mengen met andere producten. Gebruik herbruikbare medische hulpmiddelen niet als ze door het product zijn aangetast. [NL]
Avant toute utilisation, vérifier la date de péremption figurant sur l'étiquette. [FR] - Überprüfen Sie vor jeder Verwendung das auf dem Etikett angegebene Verfallsdatum. [DE] - Controleer voor elk gebruik de houdbaarheidsdatum op het etiket. [NL]
Primary placement in Belgium; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| BelgiumPrimary placement | Jul 25, 2025 | Still on market |
FR-MF-000000367The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
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 →326824F3429-01YGOn the marketEXEOL SURF 60 12X1L326824F3293-04YXOn the marketEXEOL SURF OPTIMAL 12X750ML326824F3324-01WYOn the marketEXEOL SURF OPTIMAL 12X750ML MAT326824F3324-01WYOn the marketEXEOL WIPES 60 12X100326824F3293-05YZOn the marketEXEOL WIPES OPTIMAL 12X100326824F3324-02X2On the marketNo 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 →