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ADVANCED MEDICAL SYSTEMS GROUP S.R.L.

Italy·IT-MF-000036848

Last updated September 18, 2026

About

Ams Group is responsible for producing and distributing electromedical devices capable of improving the quality of life of patients and helping doctors.

Translated from the manufacturer's own website. Source

What ADVANCED MEDICAL SYSTEMS GROUP S.R.L. makes

The company manufactures connection cables for electromedical devices and the RESALOON, a device designed for medical procedures. These products are intended for use in clinical settings to facilitate electrical connectivity and specific therapeutic applications.

The portfolio includes Class I and Class IIa devices, all of which are listed in the EU’s eudamed registry. The manufacturer is based in Italy.

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 Advanced Medical Systems Group S.R.L. manufacture?

Advanced Medical Systems Group S.R.L. primarily manufactures connection cables for electromedical devices and the RESALOON, which is designed for specific medical procedures. These products are intended for clinical use to ensure proper electrical connectivity and therapeutic functionality. The company’s portfolio includes both simple connection cables and more specialized devices like the RESALOON.

Where is Advanced Medical Systems Group S.R.L. based?

The company is based in Italy, as indicated by its country of origin. This location aligns with its participation in the EU’s regulatory framework, including the eudamed registry.

Which regulatory registries list the devices manufactured by Advanced Medical Systems Group S.R.L.?

The devices produced by Advanced Medical Systems Group S.R.L. are listed in the eudamed registry, which is the EU’s central database for medical devices. This registry ensures transparency and traceability of devices authorized for use within the European market.

How are the devices manufactured by Advanced Medical Systems Group S.R.L. classified under EU regulations?

The company’s devices fall into Class I and Class IIa classifications under EU medical device regulations. Class I devices are generally low-risk, non-invasive items like connection cables, while Class IIa devices carry a slightly higher risk and require additional safety measures, such as the RESALOON. Classification determines the regulatory requirements for authorization and post-market surveillance.

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

Information

Country
Italy
Address
12, Europa, San Pietro Viminario (Padova), Italy
Facebook
—
Phone
+39 0429719378
PRRC Contact
Francesco Sgarbi
EUDAMED SRN
IT-MF-000036848
FDA FEI Number
—
DUNS Number
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Catalogue (11)

DeviceModel / ReferenceRegistriesClassStatus
Cavi di connessione AMS-200-ST
EUDAMED
Class IActive
Cavi di connessione VE-Y-NE
EUDAMED
Class IActive
Cavi di connessione VE-Y-ST
EUDAMED
Class IActive
Resaloon 1438041/R
EUDAMED
Class IIaActive
Cavi di connessione VE-Y-BA
EUDAMED
Class IActive
Resaloon R-LOON-03
EUDAMED
Class IIaActive
Cavi di connessione VE-100-BA
EUDAMED
Class IActive
Cavi di connessione AMS-200-RA
EUDAMED
Class IActive
Cavi di connessione AMS-200-NE
EUDAMED
Class IActive
Resaloon 1267036
EUDAMED
Class IIaActive
Cavi di connessione VE-Y-RA
EUDAMED
Class IActive

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