S.S. Ent.
Country not established
- Devices
- 1
What S.S. Ent. makes
S.S. Ent. manufactures the VIVAMED Fistula Needle, a device designed for creating or accessing vascular access pathways, commonly used in hemodialysis patients.
The VIVAMED Fistula Needle is classified as a Class II medical device in the U.S. and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Vivamed Fistula Needle Ref K903440
510(k) 510(k)
Frequently asked questions
How many devices does S.S. Ent. have in the registry?
The registry currently lists 1 device for S.S. Ent.. Devices recorded under merged duplicate company entries are counted once.
Which registries list S.S. Ent.'s devices?
Among its 1 most recently registered device, S.S. Ent. has devices listed in FDA 510(k) (1 device).
What risk classes do S.S. Ent.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for S.S. Ent.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from S.S. Ent. in the registry?
The most recently registered devices listed for S.S. Ent. include VIVAMED FISTULA NEEDLE.