Neich Medical (Shenzhen) Company Limited
ChinaFDA applicant, unverified
- Devices
- 3
What Neich Medical (Shenzhen) Company Limited makes
Neich Medical produces diagnostic and interventional catheters, including the SAFFRON NM Guiding Catheter for vascular procedures and the CREATION NM Diagnostic Catheters for diagnostic imaging in cardiovascular applications.
These devices are classified as Class II under US regulations and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Saffron Nm Guiding Catheter Ref K030715
Regimes: 510(k) Registry: 510(k)Neich Nm Advance Catheter Sheath Introducer Ref K020964
Regimes: 510(k) Registry: 510(k)Creation Nm Diagnostic Catheters Ref K032888
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neich Medical (Shenzhen) Company Limited have in the registry?
The registry currently lists 3 devices for Neich Medical (Shenzhen) Company Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neich Medical (Shenzhen) Company Limited's devices?
Among its 3 most recently registered devices, Neich Medical (Shenzhen) Company Limited has devices listed in FDA 510(k) (3 devices).
What risk classes do Neich Medical (Shenzhen) Company Limited's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Neich Medical (Shenzhen) Company Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neich Medical (Shenzhen) Company Limited in the registry?
The most recently registered devices listed for Neich Medical (Shenzhen) Company Limited include SAFFRON NM GUIDING CATHETER, NEICH NM ADVANCE CATHETER SHEATH INTRODUCER and CREATION NM DIAGNOSTIC CATHETERS.