Compresses nonsterile 25 x 12 24 plys á50 pcs

Nom de l'organisation

Lola Ribar d.o.o. za proizvodnju saniteta

SRN

HR-MF-000018260

Statut du fabricant

Actif

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

• CW999

  Non-sterile product intended for external wounds. Must be sterilised before use. Product is not to be used if the packaging is damaged or the product is visibly unclean. The appropriate packaging for the sterilisation process and the cleanliness of the product during the preparation for sterilisation are to be provided by the healthcare institution. The process of product packaging and its sterilisation are to be carried out using validated methods.Single use only. Do not reuse. Once sterilised, do not resterilise. The edges of the prepared products must be free of loose threads during use. Visible damage to the gauze weave – do not use. Comply with the mandatory hospital procedures of counting medical products before and after use. Do not use after the expiration date. Comply with the mandatory procedures for the disposal of used medical products in accordance with the national laws

Marché principal en Croatie ; disponible dans 1 pays au total.

Dénomination commerciale

Compresses nonsterile 25 x 12 24 plys á50 pcs

Code d'UDI-DI

03858881103153

Basic UDI-DI

3858890791NESTLR

Numéro de référence/catalogue

1189

Entité d'attribution

GS1

Catégorie de risque

Classe I

Législation applicable

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

Statut

Sur le marché

Quantité

1

Description complémentaire du produit

Prodajna jedinica sadrži 50 komada. Hidrofilna bijela gaza, kemijski neutralna, krojena i slagana u raznim veličinama i slojevima. Obvezno sterilizirati prije upotrebe. Komprese su namijenjene za upijanje krvi i iscjetka. Prethodno sterilizirane, koriste se tijekom operacije te previjanja poslijeoperacijskih rana. Koriste se i za obradu širokog raspona vanjskih i površinskih rana.

URL des informations complémentaires

Aucune URL d'informations complémentaires renseignée par le fabricant.

Dimensions cliniques

• ±0,5cm

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

• M0201020102COTTON GAUZES, FOLDED, WITHOUT X-RAY DETECTABLE THREAD, NON-STERILE