International Medical Devices Database

Manufacturer Address
Ventus Medical, Inc., 1301 Shoreway Rd Ste 340, Belmont CA 94002-4155
Manufacturer Parent Company (2017)
Ventus Medical Inc.
Source
USFDA
1 Event
- Recall of Device Recall Nasal Cannula Diagnostic Kit

One device in the database

Device Recall Nasal Cannula Diagnostic Kit

Model / Serial
Catalog Number: MRS0208 Lot Number: 1880783
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Product was distributed in the US through a single distribution supplier.
Product Description
The Provent Nasal Cannula is a nasal appliance device placed in both nostrils intended to be used for transmission of respiratory airflow signals between the Provent Professional Sleep Apnea Therapy device and physiologic recorders.

One manufacturer with a similar name

Learn more about the data here

Ventus Medical, Inc.

Manufacturer Address
Ventus Medical, Inc., 1301 Shoreway Rd Ste 425, Belmont CA 94002-4154
Manufacturer Parent Company (2017)
Ventus Medical Inc.
Source
USFDA

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

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