Vitromed Langenfeld
GermanyFDA 510(k) applicant, unverified
- Devices
- 1
What Vitromed Langenfeld makes
Vitromed Langenfeld manufactures the V-HEPES PLUS, a buffered electrolyte solution designed for use in medical diagnostics and laboratory testing, particularly in cell culture and biochemical assays.
The V-HEPES PLUS is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
V-Hepes Plus Ref K213293
510(k) 510(k)
Frequently asked questions
How many devices does Vitromed Langenfeld have in the registry?
The registry currently lists 1 device for Vitromed Langenfeld. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vitromed Langenfeld's devices?
Among its 1 most recently registered device, Vitromed Langenfeld has devices listed in FDA 510(k) (1 device).
What risk classes do Vitromed Langenfeld's devices fall under?
Among its 1 most recently registered device, the classes recorded for Vitromed Langenfeld's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vitromed Langenfeld in the registry?
The most recently registered devices listed for Vitromed Langenfeld include V-HEPES PLUS.