Swemed Lab Intl.
Country not established
- Devices
- 1
What Swemed Lab Intl. makes
Swemed Lab Intl. manufactures the SWEMED Needle Guide, a device designed to assist in precise needle placement for medical procedures.
The SWEMED Needle Guide is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Swemed Needle Guide Ref K925999
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Swemed Lab Intl. have in the registry?
The registry currently lists 1 device for Swemed Lab Intl.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Swemed Lab Intl.'s devices?
Among its 1 most recently registered device, Swemed Lab Intl. has devices listed in FDA 510(k) (1 device).
What risk classes do Swemed Lab Intl.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Swemed Lab Intl.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Swemed Lab Intl. in the registry?
The most recently registered devices listed for Swemed Lab Intl. include SWEMED NEEDLE GUIDE.