Statistics for Laboratoires Gilbert

14Total Devices

9Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

3Countries

Certificate health for Laboratoires Gilbert

No certificates registered for this manufacturer.

Showing 1–14 of 14 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
A-CERUMEN Hygiène des oreilles	`606072`	`03518646060724`	1	On the market
A-CERUMEN Hygiène des oreilles	`606071`	`03518646060717`	1	On the market
MARIMER BABY Rhume Rhinopharyngite	`667143`	`03518646671432`	1	On the market
MARIMER Hygiène nasale quotidienne	`667138`	`03518646671388`	1	On the market
MARIMER Rhume Rhinopharyngite	`667139`	`03518646671395`	1	On the market
PARASIDOSE Lice and nits care treatment	`604287`	`03518646042874`	1	On the market
604326	`604326`	`03518646043260`	1	On the market
604325	`604325`	`03518646043253`	1	On the market
PARASIDOSE Soin traitant anti-poux et lentes	`604282`	`03518646042829`	1	On the market
PARASIDOSE Soin traitant anti-poux et lentes	`604281`	`03518646042812`	1	On the market
PHYSIODOSE Mouche bébé avec filtre	`626708`	`03518646267086`	1	On the market
PHYSIODOSE Sérum physiologique	`626737V1`	`03518646267376`	30	On the market
PHYSIODOSE Sérum physiologique	`626725V1`	`03518646267253`	30	On the market
PHYSIODOSE sérum physiologique stérile	`626663`	`03518646266638`	1	On the market

Devices placed in 3 countries

EUDAMED update: Mar 12, 2026

FR-MF-000001710

Active

FONTAINE Franck
Responsible for ensuring that the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released.
Hidden
CASTELLOTE Marine
Responsible for ensuring that: - the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; - the post-market surveillance obligations are complied with in accordance with Article 10(10); - the reporting obligations referred to in Articles 87 to 91 are fulfilled; - in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.
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