Medimex Holfeld GmbH & Co.
Country not established
- Devices
- 1
What Medimex Holfeld GmbH & Co. makes
Medimex Holfeld GmbH & Co. manufactures spinal and epidural anesthesia administration sets, including the EPISTAR and EPISTAR CSE models, designed for controlled delivery of local anesthetics during surgical procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medimex Holfeld GmbH & Co. have in the registry?
The registry currently lists 1 device for Medimex Holfeld GmbH & Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medimex Holfeld GmbH & Co.'s devices?
Among its 1 most recently registered device, Medimex Holfeld GmbH & Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Medimex Holfeld GmbH & Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medimex Holfeld GmbH & Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medimex Holfeld GmbH & Co. in the registry?
The most recently registered devices listed for Medimex Holfeld GmbH & Co. include EPISTAR/EPISTAR CSE SPINAL/EPIDURAL ANESTHESIA ADMINISTRATION SETS.