PHILIPS V30 Auto Noninvasive Auto Titrating Airway Management Device User Guide

PHILIPS V30 Auto Noninvasive Auto Titrating Airway Management Device

Product Information

Specifications

• Product Name : Philips Respironics V30 Auto BiPAP
• Part Numbers : 1135427, 1111178, 1143671
• Description : BiPAP V30 Auto mobility bundle (includes V30 Auto, roll stand, detachable battery pack and detachable battery pack enclosure), BiPAP V30 Auto (includes ventilator, power cord, and clinical manual), BiPAP V30 Auto Core

Product Usage Instructions

V30 Auto BiPAP Device

The Philips Respironics V30 Auto BiPAP device is a versatile ventilator designed to provide support for patients with respiratory issues. Follow the steps below to properly use the device

1. Ensure the device is connected to a power source using the provided power cord.
2. Refer to the clinical manual for specific instructions on setting up the device for your patient’s needs.
3. Attach any necessary accessories, such as masks or tubing, according to the patient’s requirements.
4. Power on the device and adjust the settings based on the prescribed therapy parameters.
5. Monitor the patient’s response and make any necessary adjustments to the settings as directed by a healthcare professional.
6. Regularly clean and maintain the device according to the guidelines provided in the user manual.

High Flow Therapy (HFT) on V60 and V60 Plus

The High Flow Therapy (HFT) software option has been removed from all V60 and V60 Plus devices in the US. Please follow these instructions

1. Do not use the High Flow Therapy (HFT or HFT60) software option on the V60 or V60 Plus ventilators.
2. Refer to alternative therapy options recommended by a healthcare professional.
3. For more information, visit www.Philips.com/hft-removal.

FAQ

• Q: Where can I find more information about the PE-PUR Foam voluntary recall/FSN?
  A: For information about the PE-PUR Foam voluntary recall/FSN, please visit our clinicians information page regularly for the most current information for you and your patients.

• Q: Where can I find information about Philips Respironics masks and magnets?
  A: If you have additional questions about Philips Respironics masks and magnets, please learn more here.

• Q: Where can I find the latest ventilation news and updates?
  A: For the latest ventilation news and updates, please visit our ventilation page here.

• Q: How long will service parts and bench repair services be available for the V30 Auto device?

• A: Service parts and bench repair services for the V30 Auto device will be available for purchase for five years (through December 2028), as long as components remain available.

• Q: Is the V30 Auto BiPAP device still being sold?
  A: No, as of October 31, 2023, Philips has discontinued the sale of the Philips Respironics V30 Auto BiPAP device due to product lifecycle planning.

• Q: Will valid service contracts and warranty claims be honored for the V30 Auto device?
  A: Yes, Philips will continue to honor valid service contracts and warranty claims for the V30 Auto device.

Clinical Bulletin #18

We are committed to supporting clinicians through the complete remediation process and will provide a range of resources to help you better inform, instruct, and support your patients. The clinical bulletin will continue to offer news and updates on the PE-PUR foam voluntary recall/FSN and will also be expanded to help address common topics and concerns on additional topics.
Please find below some recent information that we wanted to bring to your attention.

Ventilation Updates

V30

• As of October 31, 2023 Philips has discontinued the sale of the Philips Respironics V30 Auto BiPAP device due to product lifecycle planning.
• We will continue to honor valid service contracts and warranty claims. As such, we will make service parts and bench repair services for the V30 Auto device available for purchase for five years (through December 2028), as long as components remain available.

High flow therapy on the V60 and V60 Plus

1. As a reminder, High Flow Therapy (HFT) on the V60 or V60 Plus ventilators after November 7, 2023 is not to be used.
2. Philips Respironics is complying with the FDA’s Transition Plan for Medical Devices That Fall Within Enforcement Policies Issued During the Coronavirus Disease 2019 (COVID-19) Public Health
3. Emergency guidance document, by removing the high flow therapy (HFT or HFT60) software option from all V60 and V60 Plus devices in the US.
4. For more information, please visit www.Philips.com/hft-removal.

• Useful Links
  PE-PUR Foam voluntary recall/FSN – Information for Clinicians Be sure to visit our clinicians information page regularly for the most current information for you and your patients

• Masks and Magnets
  Have additional questions about Philips Respironics masks and magnets? Learn more here.

• Ventilation
  For the latest ventilation news and updates, please visit this page.

• For more information, visit Philips.com/src-update

References

• V60 and V60 Plus ventilators removal of the high flow therapy software option
• Information for Physicians and other medical care providers​ | Philips
• Rest Assured - Masks | Philips Healthcare
• Ventilation news and updates | Philips

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