MRMB-01

Organization name

Medical Respiratory Devices S.L

SRN

ES-MF-000000824

Manufacturer status

Active

1 warning recorded — scroll inside the panel to see all entries.

• 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.Single use only for single patient procedure. Never reuse the mounth piece even with the same patient. Re-use the rubber mouthpiece can cause product deformation. 3.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. 4. Not for use in patients known to be allergic to any of the device components.

Primary placement in Spain; available across 10 countries total.

Trade name

not provided

UDI-DI code

08436557230805

Basic UDI-DI

843655723NEUMOBITG6

Reference / catalog number

MRMB-01

Issuing entity

GS1

Risk category

Class I

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

Boquilla de goma para pruebas funcionales respiratorias

Additional information URL

https://www.medicalrd.com/

Clinical sizes

No clinical sizes registered for this device.

• Z12150185SPIROMETRY INSTRUMENTS - CONSUMABLES

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification