Vitalograph celebrates 60th anniversary

Bernard Garbe and Frank Keane outside of Vitalograph Business Park in Maids Moreton

Vitalograph reflects on extraordinary journey to becoming a global leader in respiratory diagnostics as the family-owned business celebrates its 60th Anniversary.

Vitalograph and MedM Enhance Remote Respiratory Monitoring

Lung Monitoring at Home with Vitalograph and MedM Health App

Vitalograph has joined forces with MedM Inc. to further enhance patient respiratory monitoring experience with digital health capabilities. The MedM health monitoring app is paired with Vitalograph’s Asthma-1 BT and Lung Monitor BT Smart devices.

Vitalograph Partners with NIOX to offer FeNO

feNO and spirometry puzzle

Vitalograph is proud to announce that it has become a FeNO by NIOX® UK channel partner.
Spirometry and FeNO present physicians with complementary diagnostic data to inform asthma care pathways.

The New Vitalograph Alpha Available Now

We are excited to announce the much-anticipated arrival of the new Vitalograph Alpha Spirometer – the all in one spirometer and printer with ERS/ATS 2019 compliance as standard.
This is your go anywhere spirometer, designed for testing on the go, remotely or in clinic, the Alpha is our ultimate desktop spirometry solution.

Reflecting on Medica

We were at the very first Medica trade fair in Düsseldorf, showcasing our innovative spirometry technology. Both Medica and Vitalograph have come a long way since 1968.

Product News: Introducing Spirotrac 6

We are happy to announce the launch of the next generation
Spirotrac®6 PC software which provides a powerful respiratory diagnostic platform. This redesigned software is compliant with 2019 ATS/ERS spirometry guidelines, meeting international guidelines on accuracy and reporting.

COVID-19 Virus: Vitalograph Statement

A message from our CEO:
Vitalograph’s manufacturing site is based in Ireland and has experienced little or no disruption to output during the pandemic and we are not experiencing any unmanageable supply chain disruption due to Covid-19. As a global company, we have warehouses in multiple countries holding adequate levels of stock to meet current, and anticipated, customer needs.

Vitalograph’s CE Mark is Changing

For medical devices, CE Marking indicates that products have been produced to conform to the standard required for devices sold in the EU. The CE mark is a legal requirement in order to place a medical device on the market in the EU. It is validated by a certificate issued by a notified body.

Up until 2019, Vitalograph’s CE certification was issued by a UK notified body. Due to Brexit, there is a possibility that CE certificates issued by UK notified bodies may not be valid for placing products on the EU market. To prevent complications, Vitalograph opted to change its notified body from BSI UK to BSI Netherlands.

Our notified body number has now changed from BSI UK (0086) to BSI-NL (2797). We are in the process of updating our products, packaging and documentation to reflect the change in CE Mark details. During the transition, you may see either CE Mark on our products and documentation. Regardless, our products continue to meet the same high standards and are approved for the EU market.

The relevant certification confirming the CE mark change is shown below. If you have any queries or concerns, please contact us.

| CE 00772 Certification |