A3-212-400

Dénomination commerciale

non renseigné

Code d'IUD-ID

08059304700019

IUD-ID de base

805930470A06SMALLA9

Numéro de référence/catalogue

A3-212-400

Entité d'attribution

GS1

Catégorie de risque

Classe IIb

Législation applicable

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

Statut

Sur le marché

Quantité

1

Description complémentaire du produit

Medical device designed for the disinfection and sterilization of medical devices by means of dry heat (hot air) at controlled temperature. The device enables the thermal treatment of instruments, ensuring the destruction of microorganisms through exposure to high temperatures, in accordance with the set parameters.

URL des informations complémentaires

https://www.titanox.it/

Dimensions cliniques

Aucune dimension clinique enregistrée pour ce dispositif.

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

• Z12011307DRY AIR STERILISERS

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

• CW999

  Use of the device is restricted to qualified healthcare personnel trained in dry heat sterilization processes. Do not use in the presence of explosive gases or vapors. Do not spill liquids onto the device. Do not open the door until the internal temperature has dropped below 30°C. Use heat-insulating gloves to avoid burns. Only load devices compatible with high temperatures (≥300°C) and completely dry. Do not load plastic or textile materials, or materials with an unknown melting point or a melting point below the specified limits. Ensure that all instruments are clean and dry before the cycle. Disconnect from the mains before cleaning or maintenance operations. Use only original spare parts. Maintain a minimum distance of 30 cm from portable RF equipment to avoid interference.

Aucun certificat ne référence l'IUD-ID de base de ce dispositif.