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EUDAMED last updated this device on Jul 31, 2026
B-05010724011638Stérimar HYGIENA NOSA 100 mL is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Sofibel. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
050107240116385010724011638(01)05010724011638
European Medical Device Nomenclature — the EU product classification assigned to this device.
Q030103NASAL IRRIGATION SOLUTIONSFR-MF-00000319215382Primary placement in France; available across 3 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Jan 1, 2019 | Still on market |
| Czechia | Jan 1, 2024 | Still on market |
| Slovakia | Jan 1, 2024 | Still on market |
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 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.B-03331300001204On the marketStérimar Higiene Nasal bebe 100 mLB-08470001843340On the marketStérimar Higiene Nasal bebe 50 mLB-03331300001167On the marketStérimar HYGIENA NOSA baby 50 mLB-03331300097801On the marketStérimar Igiene del naso 100 mLB-03331300007848On the marketStérimar Igiene del naso 50 mLB-03331300012118On the marketNo certificate specifically references this device's Basic UDI-DI.