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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

MARIMER Hygiène nasale quotidienne — Class IIa MDD

MD Atlas
Laboratoires Gilbert

EUDAMED last updated this device on Apr 17, 2023

MARIMER Hygiène nasale quotidienne

B-03518646671388

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Laboratoires Gilbert
UDI-DI code: 03518646671388
Reference / catalog number: 667138

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Manufacturer information

Organization name: Laboratoires Gilbert
SRN: FR-MF-000001710
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW999
Contre-indications : Ne pas utiliser chez les prématurés. Ne pas utiliser en cas d'hypersensibilité à l'eau de mer. Mises en garde : Si les symptômes persistent ou s'accentuent, consultez votre médecin. Veuillez rapporter tout incident grave survenu en lien avec ce dispositif aux Laboratoires Gilbert - site internet : www.labogilbert.fr et/ou à l'Autorité Compétente nationale. Tenir hors de la vue et de la portée des enfants.

Market distribution

Primary placement in France; available across 2 countries total.

Country	On market since	Until
FrancePrimary placement		Still on market
Belgium		Still on market

Device identification

Trade name: MARIMER Hygiène nasale quotidienne
UDI-DI code: 03518646671388
Basic UDI-DI: B-03518646671388
Reference / catalog number: 667138
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 100 MU48

EMDN nomenclature code(s)

Q030103NASAL IRRIGATION SOLUTIONS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

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Certificates

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.