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Endostart s.r.l.

Italy IT-MF-000015999 Last updated 21 Oct 2026

Devices
3
Registries
EUDAMED
FDA recalls
0

Catalogue3

About

Endostart is a startup founded in 2018 for the development and manufacturing of new generation medical devices for gastrointestinal endoscopy

From the manufacturer's own website. Source

What Endostart s.r.l. makes

Endostart manufactures the Endorail System and Endorail Set, which are designed for use in gastrointestinal endoscopy procedures. These devices are intended to assist in the insertion and navigation of endoscopes within the digestive tract, improving procedural efficiency and patient comfort.

The company’s products fall under Class I medical devices and are registered in the EU’s eudamed database. Endostart is based in Italy and adheres to EU regulatory requirements for these devices.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Endostart s.r.l. manufacture?

Endostart s.r.l. manufactures medical devices specifically designed for gastrointestinal endoscopy. Their primary products include the Endorail System and the Endorail Set, which are intended to aid in the insertion and navigation of endoscopes during procedures within the digestive tract. These devices are developed to enhance procedural efficiency and patient comfort.

Where is Endostart s.r.l. based?

Endostart s.r.l. is based in Italy. The company’s location aligns with its focus on developing and manufacturing medical devices in compliance with EU regulatory standards.

Which regulatory registries list Endostart’s medical devices?

Endostart’s medical devices are listed in the EU’s eudamed database. This registry is used to track and provide transparency on medical devices authorized within the European Union.

How are Endostart’s medical devices classified under EU regulations?

Endostart’s devices, such as the Endorail System and Endorail Set, are classified as Class I medical devices. This classification is determined based on their intended use and risk profile, with Class I devices generally posing the lowest risk and requiring less stringent regulatory oversight.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Italy
Address
265, via delle regioni , Certaldo, Italy
Phone
+39 0571843033
PRRC contact
Marco Freddolini
EUDAMED SRN
IT-MF-000015999