1534N03

Nom de l'organisation

Medical Respiratory Devices S.L

SRN

ES-MF-000000824

Statut du fabricant

Actif

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• CW999

  Warnings: 1. In case of any serious incident that has occurred in relation to the device, It should be reported to the manufacturer and the competent authority of the Member State in which the user and/or patient is established. For more report information see: https://health.ec.europa.eu/medical-devices-sector/new-regulations/contacts_en. 2. Verify that the diameter of the filter connection matches the diameter of the pulmonary function testing equipment. 3. Store filters in a clean, dry environment away from sources of heat or direct light. Handle the device with clean hands to avoid contamination. Users are recommended to wear disposable gloves when handling the filter. 4. Before use, verify that the device is not damaged, perforated or contaminated. Discard filters with any signs of damage or deterioration. 5. Incorrectly placing the filter in the pulmonary function testing equipment may result in inaccurate readings or lack of adequate protection against contamination 6. The duration of regular PFT are around 15-20 minutes. 7. Dispose of the device at the end of its useful life in accordance with local regulations on medical device waste. Do not waste it in general waste, as it may represent a risk to health and the environment.
• CW999

  Precautions: 1. The filter, nose clip and mouthpiece are disposable intended for one patient during single pulmonary function testing. They should not be reused even for the same patient in different pulmonary function test, as this increases the risk of cross-contamination and may compromise the filter's effectiveness. 2. The filter neither the nose clip and mouthpiece cannot be cleaned or sterilized after use. Device should be discarded after the PFT procedure. Contraindications: 1. Potential relative and absolute contraindications for the pulmonary function testing (PFT) should be evaluated carefully by healthcare professional for particular patient. 2. Patients with pacemakers do not have an absolute contraindication to lung function testing However, it is important to inform the physician about the presence of the pacemaker before performing the lung function test. 3. Not for use in patients known to be allergic to any of the device components.

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

Dénomination commerciale

non renseigné

Code d'UDI-DI

08436557231086

Basic UDI-DI

843655723NEUMOFILTPPSK

Numéro de référence/catalogue

1534N03

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

Neumofilt Ergo Pack Plus

URL des informations complémentaires

https://www.medicalrd.com/

Dimensions cliniques

• 34 MU50
• 37.5 MU50

• R049001PULMONARY FUNCTION TEST FILTERS

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