EUDAMED a mis à jour ce dispositif le 31 août 2026

CONTACTA OCCHI SECCHI GEL INTENSO MONODOSE

80336618004020200000000Q6

Sur le marchéClasse IIb

Législation applicable: MDR [Règlement (UE) 2017/745 relatif aux dispositifs médicaux]
Nom de l'organisation: Fidia Farmaceutici S.p.A.
: 08055267244133
Numéro de référence/catalogue: 13002017

Voir la famille de dispositifs (IUD de base)

CONTACTA OCCHI SECCHI GEL INTENSO MONODOSE est un dispositif médical relevant du règlement européen MDR, enregistré dans EUDAMED. Il est classé en Classe IIb. Fabriqué par Fidia Farmaceutici S.p.A.. Commercialisé sur le marché européen en Italie. Découvrez les certificats, le statut réglementaire et la fiche EUDAMED sur DM Atlas.

Identification du dispositif

Dénomination commerciale: CONTACTA OCCHI SECCHI GEL INTENSO MONODOSE
: 08055267244133
: 80336618004020200000000Q6
Numéro de référence/catalogue: 13002017
: GS1

Classification

: Classe IIb
Législation applicable: MDR [Règlement (UE) 2017/745 relatif aux dispositifs médicaux]
Statut: Sur le marché

Détails sur le dispositif

Quantité: 1
Description complémentaire du produit: —
URL des informations complémentaires: Aucune URL d'informations complémentaires renseignée par le fabricant.
Dimensions cliniques: 0.35 MU48

Traçabilité IUD-IP

Numéro de lot
Date d'expiration
Date de fabrication
Numéro de série
Identification du logiciel

DataMatrix IUD-ID

Encodé

(01)08055267244133

Code(s) de la nomenclature (EMDN)

Nomenclature européenne des dispositifs médicaux — la classification produit UE attribuée à ce dispositif.

Q02030206EYE LUBRICANT SOLUTIONS

Avertissements critiques

1 avertissement enregistré — faire défiler le panneau pour tout voir.

• The product is for ophthalmic external use only (eye surface). • In order to avoid the risk of cross-infection, the product is intended to be used by a single patient only. • To avoid contaminating the solution, do not allow the single-dose container to come into contact with the eye or other objects. • To avoid damage to the ocular surface, do not allow the single-dose container to come into contact with the eye while instilling the product. • The product is in single-dose packaging. After administration, the sealed single-dose container with the remaining content should be disposed of in accordance with local requirements. • The product is in single-dose packaging. The volume contained in the single-dose container is for a single administration, since the product does not contain preservatives. Reuse of the residual content may cause ophthalmic infection and/or patient injury. • No interactions of CONTACTA OCCHI SECCHI GEL INTENSO MONODOSE with drugs or other topical ophthalmic products are known; however, consult your physician in case of concomitant administration with other topical ophthalmic products for specific indications on timing of administration. • Do not use the product if the single-dose container or the aluminium pouch are damaged. • Keep the product out of sight and reach of children. • In case of any undesirable effects, discontinue use and seek medical advice. • Keep the box and the leaflet for the entire period of use of the device.
AUTRE

Indicateurs de conformité

Sécurité

Substances

Réglementaire

Cycle de vie

English

Avertissements critiques

1 avertissement enregistré — faire défiler le panneau pour tout voir.

• The product is for ophthalmic external use only (eye surface). • In order to avoid the risk of cross-infection, the product is intended to be used by a single patient only. • To avoid contaminating the solution, do not allow the single-dose container to come into contact with the eye or other objects. • To avoid damage to the ocular surface, do not allow the single-dose container to come into contact with the eye while instilling the product. • The product is in single-dose packaging. After administration, the sealed single-dose container with the remaining content should be disposed of in accordance with local requirements. • The product is in single-dose packaging. The volume contained in the single-dose container is for a single administration, since the product does not contain preservatives. Reuse of the residual content may cause ophthalmic infection and/or patient injury. • No interactions of CONTACTA OCCHI SECCHI GEL INTENSO MONODOSE with drugs or other topical ophthalmic products are known; however, consult your physician in case of concomitant administration with other topical ophthalmic products for specific indications on timing of administration. • Do not use the product if the single-dose container or the aluminium pouch are damaged. • Keep the product out of sight and reach of children. • In case of any undesirable effects, discontinue use and seek medical advice. • Keep the box and the leaflet for the entire period of use of the device.
AUTRE

CONTACTA OCCHI SECCHI GEL INTENSO MONODOSE

Identification du dispositif

Classification

Détails sur le dispositif

Traçabilité IUD-IP

DataMatrix IUD-ID

Code(s) de la nomenclature (EMDN)

Avertissements critiques

Indicateurs de conformité

Sécurité

Substances

Réglementaire

Cycle de vie

Identification du dispositif

Classification

Détails sur le dispositif

Informations sur le fabricant

Traçabilité IUD-IP

DataMatrix IUD-ID

Code(s) de la nomenclature (EMDN)

Avertissements critiques

Indicateurs de conformité

Sécurité

Substances

Réglementaire

Cycle de vie

Certificats

Certificats couvrant ce dispositif

Dispositifs connexes

Informations sur le fabricant

DataMatrix IUD-IP

Distribution sur le marché

Recherches associées

Certificats couvrant ce dispositif

Certificats

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