0101-0110

Nom de l'organisation

Phi Med Europe

SRN

ES-MF-000029605

Statut du fabricant

Actif

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

• CW999

  WARNINGS REGARDING EMC The equipment is in conformity with the standards regarding Electromagnetic Compatibility, not causing electromagnetic disturbances, and complying with immunity standards. To prevent adverse events to the patient and Operator due to electromagnetic disturbances, the device requires the following special precautions regarding EMC: - The equipment should not be located close to other devices or stacked with other devices. - The use of accessories, transducers or cables not specified or provided by Phi Med Europe S.L. may negatively affect EMC performance. - “Portable RF communications equipment including antennas should be used no closer than 30 cm (12 inches) to any part of the device, including cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment could result” - All the mentioned warnings and instructions must be followed for maintaining basic safety with regard to electromagnetic disturbances for the expected service life. NOTE: “The EMISSIONS characteristics of this equipment make it suitable for use in industrial areas and hospitals (CISPR 11 class A). If it is used in a residential environment (for which CISPR 11 class B is normally required) this equipment might not offer adequate protection to radio-frequency communication services. The user might need to take mitigation measures, such as relocating or re-orienting the equipment”
• CW011

  Do not use the device on open wounds or mucous membranes.
• CW999

  CONTRAINDICATION • Do not use in people with pacemakers due to electromagnetic disturbances. Likewise, any medical implantation instrument that contains an RF system, if implanted, makes the application of this study not possible and in the case of being external (i.e. insulin pump), the development of the test must be done without the operation of this instrument.
• CW999

  CONTRAINDICATION Do not use the device in patient under psychiatric medical treatment or pathological cognitive status
• CW999

  CONTRAINDICATION Do not use the device on children under the age of 15 years old.
• CW999

  CONTRAINDICATION Not indicated for pregnant and nursing women.
• CW999

  WARNING Side-effect: Possible local erythema of the skin may occur.

Marché principal en Espagne ; disponible dans 10 pays au total.

Dénomination commerciale

non renseigné

Code d'UDI-DI

08437023855003

Basic UDI-DI

B-08437023855003

Numéro de référence/catalogue

0101-0110

Entité d'attribution

GS1

Catégorie de risque

Classe IIa

Législation applicable

MDD [Directive 93/42/CEE relative aux dispositifs médicaux]

Statut

Sur le marché

Quantité

1

Description complémentaire du produit

—

URL des informations complémentaires

Aucune URL d'informations complémentaires renseignée par le fabricant.

Dimensions cliniques

Aucune dimension clinique enregistrée pour ce dispositif.

• V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER

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