VICUM 2ML ECOUV. FLOQ.URETRAL 80MM FLOW

Nom de l'organisation

Deltalab, S.L.

SRN

ES-MF-000000153

Statut du fabricant

Actif

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

• CW010

  Not suitable for any other application than its intended use. Do not use if the packaging has any signs of breakage or damage. If you see that the unit package has lost its integrity, do not use the swab as there is no guarantee of its sterility. Do not use if you notice that the swab is dirty. Discard the product if you find any broken brushes, with edges or without a head. Do not use if the liquid of the transport swab with media is cloudy or seems altered. Only for single use, the reuse of this product may cause infections. Handle carefully. Any strong pressure during use, although unlikely, could break the swab. In the case of any damage, discard immediately. After use, the swabs must be decontaminated or treated as contaminated medical waste. It is the responsibility of each laboratory to handle, treat and dispose the waste according to the current legislation. Unused swabs can be considered non-hazardous products and can be disposed of accordingly. All the above is applicable to the enrichment media supplied with flocked swab. Do not use if the expiration date has been exceeded. Do not use if any component is missing or if the printed product information is not displayed correctly. Do not ingest the means of transport under any circumstances.

Marché principal en Espagne ; disponible dans 5 pays au total.

Dénomination commerciale

VICUM 2ML ECOUV. FLOQ.URETRAL 80MM FLOW

Code d'UDI-DI

08435605814981

Basic UDI-DI

84356058UDI-DI-246C

Numéro de référence/catalogue

304236KF

Entité d'attribution

GS1

Catégorie de risque

Classe IIa

Législation applicable

MDR [Règlement (UE) 2017/745 relatif aux dispositifs médicaux]

Statut

Sur le marché

Quantité

6

Description complémentaire du produit

—

URL des informations complémentaires

https://www.deltalabgroup.com/eifus

Dimensions cliniques

Aucune dimension clinique enregistrée pour ce dispositif.

• A1102SAMPLE COLLECTION SWABS WITH TRANSPORT MEDIUM

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