Uptake Medical B.V.
Netherlands NL-MF-000032434 Last updated 17 Sep 2026
- Devices
- 4
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
InterVapor® Personalized Procedure Program (IP3®) Ref UM-IP3-100
Intervapor Generator Ref UM-GEN-100
Intervapor Catheter Ref UM-CTH-100
InterVapor Drain Bag Ref UM-BAG-100
About
Uptake Medical® Technology Inc. is a medical device company based in San Jose, CA, USA. Uptake Medical is dedicated to improving the lives of patients suffering from pulmonary disease with vapor ablation.
What Uptake Medical B.V. makes
Uptake Medical B.V. manufactures medical devices for vapor ablation procedures, including the InterVapor® Personalized Procedure Program (IP3®), which coordinates system components for treatment. The portfolio includes the Intervapor Generator, a device for delivering controlled vapor, along with disposable components like the Intervapor Catheter and InterVapor Drain Bag for procedural use.
The company’s devices are classified under EU regulations as Class I, Class IIa, and Class IIb, with all relevant products registered in the EU’s eudamed database. The manufacturer is based in the Netherlands and adheres to regulatory requirements for medical devices within the European Union.
Frequently asked questions
What types of medical devices does Uptake Medical B.V. manufacture?
Uptake Medical B.V. manufactures medical devices specifically designed for vapor ablation procedures. These include the InterVapor Generator, which delivers controlled vapor, and disposable components like the Intervapor Catheter and InterVapor Drain Bag. The company also offers the InterVapor® Personalized Procedure Program (IP3®), a system that integrates these components to coordinate treatment. These devices are intended to assist in procedures related to pulmonary disease.
Where is Uptake Medical B.V. based, and what regulatory region does it operate in?
Uptake Medical B.V. is based in the Netherlands. The company operates within the European Union regulatory framework, ensuring its devices comply with EU medical device regulations. This includes registration in the EU’s official database, eudamed, where relevant products are listed for transparency and traceability.
How are Uptake Medical B.V.’s devices classified under EU regulations?
Uptake Medical B.V.’s devices are classified under EU regulations as Class I, Class IIa, and Class IIb. The classification determines the level of scrutiny and regulatory requirements for each device type. For example, Class IIb devices typically involve a higher risk and require more rigorous evaluation compared to Class I devices, which pose minimal risk. The specific classification for each product depends on its intended purpose and potential risks.
Are Uptake Medical B.V.’s devices listed in any regulatory registries?
Yes, Uptake Medical B.V.’s devices are listed in the EU’s eudamed database. eudamed is the official EU registry for medical devices, where manufacturers provide information about their products to ensure transparency, traceability, and compliance with EU regulations. Listing in eudamed is a requirement for devices marketed within the European Union.
What is the purpose of the InterVapor® Personalized Procedure Program (IP3®) in the company’s device portfolio?
The InterVapor® Personalized Procedure Program (IP3®) is a system developed by Uptake Medical B.V. that coordinates and integrates the various components used in vapor ablation procedures. It includes the Intervapor Generator, disposable catheters, and drain bags, working together to deliver controlled vapor treatments. The IP3® system is designed to enhance precision and efficiency during procedures, particularly for patients with pulmonary conditions.
Information
- Country
- Netherlands
- Address
- 114, Pettelaarpark, 's-Hertogenbosch, Netherlands
- Website
- www.uptakemedical.com
- [email protected]
- Phone
- +31 73-3032563
- PRRC contact
- Antoinette Clay
- EUDAMED SRN
- NL-MF-000032434