International Medical Devices Database

Manufacturer Address
Cardiovascular Systems Inc, 1225 Old Hwy 8 NW, Saint Paul MN 55112-6416
Manufacturer Parent Company (2017)
Cardiovascular Systems, Inc.
Source
USFDA
1 Event
- Recall of Device Recall ViperWire Advance peripheral guide wire

One device in the database

Device Recall ViperWire Advance peripheral guide wire

Model / Serial
Lot #160877, UDI Number: (01)10852528005084(17)180430(10)160877.
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
US Nationwide distribution.
Product Description
ViperWire Advance Peripheral Guide Wire, Sterilized with Ethylene Oxide, Rx Only. Part number 72023-02, Model Number VPR-GW-17. Five (5) guide wire pouches in one (1) guide wire box. For use with CSI Peripheral Orbital Atherectomy Devices (OAD), including Stealth 360 and Diamondback 360. Cardiovascular.

5 manufacturers with a similar name

Learn more about the data here

Terumo Cardiovascular Systems Inc

Manufacturer Parent Company (2017)
Terumo Corp.
Source
NZMMDSA

Cardiovascular Systems Inc

Manufacturer Address
Cardiovascular Systems Inc, 1225 Old Highway 8 NW, Saint Paul MN 55112-6416
Manufacturer Parent Company (2017)
Cardiovascular Systems, Inc.
Source
USFDA

Cardiovascular Systems Inc.

Manufacturer Parent Company (2017)
Cardiovascular Systems, Inc.
Source
BAM

Cardiovascular Systems Inc

Manufacturer Parent Company (2017)
Cardiovascular Systems, Inc.
Source
SATP

Cardiovascular systems inc.

Manufacturer Parent Company (2017)
Cardiovascular Systems, Inc.
Source
RLMPH

About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

Stories in your inbox

Do you work in the medical industry? Or have experience with a medical device? Our reporting is not done yet. We want to hear from you.

Tell us your story!

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.

Download the data

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.

Download all (zipped)