PRO-22 Automatic blood pressure monitor

Nom de l'organisation

B.Well Swiss AG

SRN

CH-MF-000012588

Statut du fabricant

Actif

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

• CW999

  Do not use this device if the patient’s condition meets the following contraindications, to avoid inaccurate measurements or injuries.
• CW999

  The device is not suitable for use on patients with implanted, electrical devices, such as cardiac pacemakers and defibrillators.
• CW999

  Avoid taking measurement on the arm on the side of a mastectomy or lymph node clearance.
• CW999

  The device measures blood pressure using a pressured cuff. If the measuring limb suffers from injuries (for example open wounds) or under conditions or treatments (for example intravenous drip) making it unsuitable for surface contact or pressurization, do not use the device, to avoid worsening of the injuries or conditions.
• CW999

  Avoid taking measurements of patients with conditions, diseases, and susceptible to environment conditions that lead to incontrollable motions (e.g. trembling or shivering) and inability to communicate clearly (for example children and unconscious patients).
• CW999

  The device uses oscillometric method to determine blood pressure. The arm being measure should have normal perfusion. The device is not intended to be used on a limb with restricted or impaired blood circulation.If you suffer with perfusion or blood disorders, consult your doctor before using the device.

Marché principal en Lituanie ; disponible dans 4 pays au total.

Dénomination commerciale

PRO-22 Automatic blood pressure monitor

Code d'UDI-DI

07640156398908

Basic UDI-DI

764015639MDA0203_2LB

Numéro de référence/catalogue

1101628

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

1

Description complémentaire du produit

PRO-22 Automatic blood pressure monitor

URL des informations complémentaires

Aucune URL d'informations complémentaires renseignée par le fabricant.

Dimensions cliniques

Aucune dimension clinique enregistrée pour ce dispositif.

• Z1203020302NON–INVASIVE BLOOD PRESSURE MONITORING INSTRUMENTS

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

Santé des certificats sur le portefeuille de ce fabricant.