Martin Uram, MD
Country not established
- Devices
- 2
What Martin Uram, MD makes
The company produces the E3 Microprobe, a medical device designed for precise tissue ablation or coagulation, and the E3 Microprobe Series of lasers and associated accessories for controlled energy delivery in surgical procedures.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The manufacturer is based in the United States.
Catalogue
E3 Microprobe Ref K974878
Regimes: 510(k) Registry: 510(k)E3 Microprob Series Of Lasers And Accessories Ref K000192
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Martin Uram, MD have in the registry?
The registry currently lists 2 devices for Martin Uram, MD. Devices recorded under merged duplicate company entries are counted once.
Which registries list Martin Uram, MD's devices?
Among its 2 most recently registered devices, Martin Uram, MD has devices listed in FDA 510(k) (2 devices).
What risk classes do Martin Uram, MD's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Martin Uram, MD's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Martin Uram, MD in the registry?
The most recently registered devices listed for Martin Uram, MD include E3 MICROPROBE and E3 MICROPROB SERIES OF LASERS AND ACCESSORIES.