Tidewave

Dénomination commerciale

Tidewave

07073196000010

7073196TWTURNINGGA

Numéro de référence/catalogue

TWTURNING

GS1

Classe I

Législation applicable

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

Statut

Sur le marché

Quantité

1

Description complémentaire du produit

Tidewave™ Mattress is designed to give the user continuous movement to prevent and treat pressure ulcers up to and including grade 4.

URL des informations complémentaires

https://tidewave.no/en/how-to-use/

Dimensions cliniques

• 9–150 MU29

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

• V080701ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES

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

• Prudence, risque de choc électrique

  The use of Tidewave™ Mattress nearby or in conjunction with other electrical equipment should be avoided, such use could cause the product to malfunction. If such use is considered necessary, the product and its auxiliary equipment should be closely monitored to confirm normal operation is maintained. Electrical equipment may be harmful if used in a manner not intended, or if the equipment is damaged. Make sure power is disconnected before any repair or maintenance work is performed to the equipment. Maintenance and repair work should only be performed by certified technicians.

• Partie appliquée de type BF

  The mattress hygiene cover is an applied part BF. The mattress hygiene cover is electrically insulated from the rest of the equipment

• Consulter un professionnel de la santé avant toute utilisation

  If the patient is mobile and likely to get out of the bed by themselves, even while the mattress is running, the use of this mattress must be risk evaluated by competent care provider before the product can be used.

• Read the user manual before product is used

  AUTRE