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EUDAMED last updated this device on Jun 29, 2026
326824F3423-01X6EXEOL SEPT E2 6X1L DOSEUR 20ML MAT 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 Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0326824005626420000002911 packaging level registered — each level carries its own UDI-DI.
03268240056264× 1 unitBase unit13268240056261× 6 units(01)03268240056264
European Medical Device Nomenclature — the EU product classification assigned to this device.
D0901AMMONIUM SALTS FOR THE DISINFECTION OF MEDICAL DEVICES16 warnings recorded — scroll inside the panel to see all entries.
Llamar inmediatamente a un CENTRO DE TOXICOLOGÍA, un médico. [ES] - Contacte imediatamente um CENTRO DE INFORMAÇÃO ANTIVENENOS, um médico. [PT]
Recoger el vertido. [ES] - Recolher o produto derramado. [PT]
Contiene Subtilisina (CAS: 9014-01-1). Puede provocar una reacción alérgica. [ES] - Contém subtilisina (CAS: 9014-01-1). Pode provocar uma reacção alérgica. [PT]
Primary placement in Spain; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| SpainPrimary placement | May 18, 2026 | Still on market |
| Portugal | May 18, 2026 | Still on market |
FR-MF-000000367The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
OTHER
Muy tóxico para los organismos acuáticos, con efectos nocivos duraderos. [ES] - Muito tóxico para os organismos aquáticos com efeitos duradouros. [PT]
Irritación o corrosión cutáneas, categoría 1, subcategoría 1B / Lesiones oculares graves o irritación ocular, categoría 1 [ES] - Corrosão/irritação cutânea, categoria 1, subcategoria 1B / Lesões oculares graves/irritação ocular, categoria 1 [PT]
Peligroso para el medio ambiente acuático – Peligro agudo, categoría 1 / Peligroso para el medio ambiente acuático – Peligro crónico, categoría 3 [ES] - Perigoso para o ambiente aquático – perigo agudo, categoria 1 / Perigoso para o ambiente aquático – perigo crónico, categoria 3 [PT]
Provoca quemaduras graves en la piel y lesiones oculares graves. [ES] - Provoca queimaduras na pele e lesões oculares graves.[PT]
Evitar su liberación al medio ambiente. [ES] - Evitar a libertação para o ambiente. [PT]
Llevar guantes de protección, ropa de protección, equipo de protección para los ojos y la cara. [ES} - Usar luvas de protecção, vestuário de protecção, protecção ocular, protecção facial. [PT]
EN CASO DE INGESTIÓN: Enjuagar la boca. [ES] - EM CASO DE INGESTÃO: Enxaguar a boca. [PT]
EN CASO DE INGESTIÓN: NO provocar el vómito. [ES] - EM CASO DE INGESTÃO: NÃO provocar o vómito. [PT]
EN CASO DE CONTACTO CON LA PIEL (o el pelo): Quitar inmediatamente toda la ropa contaminada. [ES] - SE ENTRAR EM CONTACTO COM A PELE (ou o cabelo): Retirar imediatamente toda a roupa contaminada. [PT]
EN CASO DE CONTACTO CON LOS OJOS: Quitar las lentes de contacto cuando estén presentes y pueda hacerse con facilidad. Proseguir con el lavado. [ES] - SE ENTRAR EM CONTACTO COM OS OLHOS: Se usar lentes de contacto, retire-as, se tal lhe for possível. Continue a enxaguar. [PT]
EN CASO DE CONTACTO CON LA PIEL (o el pelo): Enjuagar la piel con agua. [ES] - SE ENTRAR EM CONTACTO COM A PELE (ou o cabelo): Enxaguar a pele com água. [PT]
EN CASO DE CONTACTO CON LOS OJOS: Enjuagar con agua cuidadosamente durante varios minutos. [ES] - SE ENTRAR EM CONTACTO COM OS OLHOS: Enxaguar cuidadosamente com água durante vários minutos. [PT]
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 →326824F3423-01X6On the marketEXEOL SEPT E2 4X5L +1 PPE 20ML MAT326824F3423-01X6On the marketEXEOL SEPT E2 6X1L DOSEUR 20ML326824F3423-01X6On the marketEXEOL SEPT FIRST 4X5L+1PP 20ML326824F3422-01WXOn the marketEXEOL SEPT FIRST 4X5L+1PP 20ML MAT326824F3422-01WXOn the marketEXEOL SEPT FIRST 6X1L DOS 20ML326824F3422-01WXOn 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 →