Sterilmed Inc. (Johnson and Johnson)
Country not established
- Devices
- 1
What Sterilmed Inc. (Johnson and Johnson) makes
Sterilmed Inc. manufactures reprocessed electrophysiology catheters, including the PentaRay Nav eco High-Density Mapping Catheter, designed for cardiac mapping procedures to guide ablation therapies.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices and is listed in the FDA’s 510(k) database. Sterilmed Inc. is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sterilmed Inc. (Johnson and Johnson) have in the registry?
The registry currently lists 1 device for Sterilmed Inc. (Johnson and Johnson). Devices recorded under merged duplicate company entries are counted once.
Which registries list Sterilmed Inc. (Johnson and Johnson)'s devices?
Among its 1 most recently registered device, Sterilmed Inc. (Johnson and Johnson) has devices listed in FDA 510(k) (1 device).
What risk classes do Sterilmed Inc. (Johnson and Johnson)'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sterilmed Inc. (Johnson and Johnson)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sterilmed Inc. (Johnson and Johnson) in the registry?
The most recently registered devices listed for Sterilmed Inc. (Johnson and Johnson) include Reprocessed PentaRay Nav eco High-Density Mapping Catheter.