International Medical Devices Database

Manufacturer Address
Cardima Inc, 47266 Benicia St, Fremont CA 94538-1372
Source
USFDA
2 Events
- Recall of Device Recall Cardima Surgical Ablation Probe (SAP)
- Recall of Device Recall Cardima Surgical Ablation Probe (SAP)

One device in the database

Device Recall Cardima Surgical Ablation Probe (SAP)

Model / Serial
Model number 01-242208
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution to Distributors in USA (Pittsburgh, PA) and the countries of Ireland and Belgium, and customers in the states of CA, OH, MI, MO, AND WA, and the countries of Ireland and the Netherlands.
Product Description
Cardima Surgical Ablation Probe (SAP) Electrosurgical cutting and coagulation device, Model Number 01-242208, manufactured by Cardima Inc, Fremont, CA

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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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Cardima Inc

One device in the database

Device Recall Cardima Surgical Ablation Probe (SAP)