Endostart SRL
Country not established FDA
Part of Endostart SRL
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Endostart SRL makes
Endostart Srl manufactures external magnetic systems and magnetic balloon catheters designed for manipulating gastrointestinal endoscopes during procedures. These tools assist in navigating and positioning endoscopes within the digestive tract, improving precision and control during diagnostic or therapeutic interventions.
The company’s products are classified as Class II medical devices under regulatory frameworks and are listed in the FDA’s Unique Device Identification (UDI) system. Endostart Srl operates from the United States, adhering to applicable regulatory standards for these specialized endoscopic accessories.
Catalogue
- CE MDR GUDID
- CE MDR GUDID
Company details
- DUNS number
- 439228695
- [email protected]
- Phone
- +390571843033
FDA establishments
- Endostart SRL Certaldo Firenze · IT FEI 3026121953
Frequently asked questions
How many devices does ENDOSTART SRL have in the registry?
The registry currently lists 2 devices for ENDOSTART SRL. Devices recorded under merged duplicate company entries are counted once.
Which registries list ENDOSTART SRL's devices?
Among its 2 most recently registered devices, ENDOSTART SRL has devices listed in FDA GUDID (2 devices).
What risk classes do ENDOSTART SRL's devices fall under?
Among its 2 most recently registered devices, the classes recorded for ENDOSTART SRL's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ENDOSTART SRL in the registry?
The most recently registered devices listed for ENDOSTART SRL include Endorail System ESYSTEMGEN2V01A and Endorail Set ESETGEN2V02A.
Which FDA establishments are linked to ENDOSTART SRL?
1 FDA establishment is linked to ENDOSTART SRL in the registry; they are listed on the company page.