Mona Terminal 2.0 series 0.1

Nom de l'organisation

Clinomic Medical GmbH

SRN

DE-MF-000013339

Statut du fabricant

Actif

3 avertissements enregistrés — faire défiler le panneau pour tout voir.

• CW011

  Misuse of the terminal can result in hazardous situations. The following is therefore essential: – Never use the terminal for mobile emergency care (e.g. ambulance). – Never allow unauthorised persons to access the terminal. – Never open the terminal’s housing. – Do not stack the terminal with other devices. – Never lay the power supply cables for other devices across the terminal or wind them around the terminal’s mounting elements.
• CW273

  Contact with live parts poses an immediate danger of fatal electric shock. Damage to the device or the power supply cable can be life-threatening. – Make sure that the building’s mains connection has a 4 kV isolation barrier (network isolator). – Only connect the device to a mains supply with a protective earth conductor. – To isolate the device from the mains supply, unplug the power supply cable. – Keep moisture away from the device and the power supply cable. Moisture can result in a short circuit. – If the device is damaged, switch it off immediately, put it out of use and arrange for repairs. – If the power supply cable is damaged, switch off the device immediately and replace the power supply cable. – Have defective devices repaired by Clinomic customer service only.
• CW010

  Observe instruction manual

Marché principal en Allemagne ; disponible dans 2 pays au total.

Dénomination commerciale

non renseigné

Code d'UDI-DI

04260735730054

Basic UDI-DI

4260735730029B

Numéro de référence/catalogue

Mona Terminal 2.0 series 0.1

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

404

Description complémentaire du produit

—

URL des informations complémentaires

https://www.clinomic.ai/ifu

Dimensions cliniques

Aucune dimension clinique enregistrée pour ce dispositif.

• Z1203020201MULTI–PARAMETER PATIENT BEDSIDE MONITORS

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

Santé des certificats sur le portefeuille de ce fabricant.