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EUDAMED last updated this device on Nov 28, 2024
326824F3422-01WXEXEOL SEPT FIRST 6X1L DOS 20ML 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.
03268240059333EXS0043FR-011 packaging level registered — each level carries its own UDI-DI.
03268240059333× 1 unitBase unit13268240059330× 6 units(01)03268240059333
European Medical Device Nomenclature — the EU product classification assigned to this device.
D0901AMMONIUM SALTS FOR THE DISINFECTION OF MEDICAL DEVICES20 warnings recorded — scroll inside the panel to see all entries.
Primary placement in France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Sep 26, 2024 | Still on market |
FR-MF-000000367The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Porter des gants de protection, des vêtements de protection, un équipement de protection des yeux et du visage.
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 →326824F3423-01X6On the marketEXEOL SEPT FIRST 4X5L+1PP 20ML326824F3422-01WXOn the marketEXEOL SEPT FIRST 4X5L+1PP 20ML MAT326824F3422-01WXOn the marketEXEOL SEPT FIRST 6X1L DOS 20ML MAT326824F3422-01WXOn the marketEXEOL SEPT FOAM 12X750ML326824F3429-01YGOn the marketEXEOL SURF 60 12X1L326824F3293-04YXOn the market