Schneider/Namic
Country not established
- Devices
- 2
What Schneider/Namic makes
Schneider/Namic manufactures vascular access devices, including introducer sheaths, dilators, obturators, and infusion introducer sets designed for procedural use in interventional radiology and cardiology. These products are intended for guiding catheters and facilitating fluid infusion during procedures such as angiography or port placement.
The company’s portfolio is regulated under Class II medical devices in the US, with devices authorised via the FDA’s 510(k) pathway. Products are listed in the FDA’s 510(k) registry, reflecting compliance with US regulatory requirements. The company operates from the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Schneider/Namic have in the registry?
The registry currently lists 2 devices for Schneider/Namic. Devices recorded under merged duplicate company entries are counted once.
Which registries list Schneider/Namic's devices?
Among its 2 most recently registered devices, Schneider/Namic has devices listed in FDA 510(k) (2 devices).
What risk classes do Schneider/Namic's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Schneider/Namic's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Schneider/Namic in the registry?
The most recently registered devices listed for Schneider/Namic include EMCEE INTRODUCER SHEATH, DILATOR, OBTURATOR, INTRODUCER SET and EMCEE INFUSION INTRODUCER SHEATH, EMCEE INFUSION INTRODUCER SET DILATOR, EMCEE INFUSION INTRODUCER SHEATH SET, EMCEE INF.