Coombs Medical Device Consulting
Country not established
- Devices
- 1
What Coombs Medical Device Consulting makes
Coombs Medical Device Consulting manufactures the ESTECH Percutaneous Insertion Dilator Kit, a surgical tool designed for controlled dilation of tissue or vessels during minimally invasive procedures.
The ESTECH Percutaneous Insertion Dilator Kit is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company operates from the United States.
Catalogue
Estech Percutaneous Insertion Dilator Kit Ref K070749
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Coombs Medical Device Consulting have in the registry?
The registry currently lists 1 device for Coombs Medical Device Consulting. Devices recorded under merged duplicate company entries are counted once.
Which registries list Coombs Medical Device Consulting's devices?
Among its 1 most recently registered device, Coombs Medical Device Consulting has devices listed in FDA 510(k) (1 device).
What risk classes do Coombs Medical Device Consulting's devices fall under?
Among its 1 most recently registered device, the classes recorded for Coombs Medical Device Consulting's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Coombs Medical Device Consulting in the registry?
The most recently registered devices listed for Coombs Medical Device Consulting include ESTECH PERCUTANEOUS INSERTION DILATOR KIT.