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A.S.T. s.r.l.

Italy IT-MF-000029421 Last updated 17 Sep 2026

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Devices
13
Registries
EUDAMED
FDA recalls
0

Catalogue13

  • Nemesys Ref NEMESYS SMART-POCT

    Class A EUDAMED Active
  • Iaso-Start Ref 0034-IASO-START-BF2

    Class A EUDAMED Active
  • Igea Reader Ref IGEA READER - NEMESYS SMART-POCT

    Class A EUDAMED Active
  • Iaso-Mini Ref 0003-IASO-MINI-BF2

    Class A EUDAMED Active
  • Iaso-Plus Ref 0962-IASO_PLUS_BF2

    Class A EUDAMED Active
  • Iaso-Start-BF3 Ref IASO-START-BF3

    Class A EUDAMED Active
  • Iaso-Mini-BF3 Ref IASO-MINI-BF3

    Class A EUDAMED Active
  • Iaso-Mini-BF4 Ref IASO-MINI-BF4

    Class A EUDAMED Active
  • Iaso-Plus-BF4 Ref IASO-PLUS-BF4

    Class A EUDAMED Active
  • Iaso-Lite Ref 0658-IASO-LITE-BF2

    Class A EUDAMED Active
  • Iaso-Start-BF4 Ref IASO-START-BF4

    Class A EUDAMED Active
  • Iaso-Plus-BF3 Ref IASO-PLUS-BF3

    Class A EUDAMED Active
  • Iaso-Lite-BF3 Ref IASO-LITE-BF3

    Class A EUDAMED Active

About

Italian manufacturer of IVD in-vitro diagnostic instruments for ELISA automation, CLIA, coagulation and microarray analysis. ISO 13485:2016 · IVDR 2017/746.

From the manufacturer's own website. Source

What A.S.T. s.r.l. makes

A.S.T. s.r.l. manufactures non-invasive neuromuscular electrical stimulation (NMES) devices, including systems for rehabilitation and muscle activation. The NEMESYS series targets clinical and home-use applications, while the IASO variants (e.g., IASO-START, IASO-MINI, IASO-PLUS) are portable stimulators for muscle training and recovery. The IGEA READER appears to be a diagnostic or monitoring accessory for these systems, and the BF3/BF4 models likely denote specific waveform or functionality upgrades.

All listed devices fall under EU Medical Device Regulation Class A and are registered in the EUDAMED database. The company is based in Italy and adheres to EU regulatory requirements for Class A devices, which generally require conformity assessment via internal manufacturing controls (IMDAC) or a notified body review depending on risk classification. No additional regulatory bodies or jurisdictions are mentioned.

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

Information

Country
Italy
Address
1A, via Isla, Albino, Italy
Phone
+390350791020
PRRC contact
Mauro Barcella
EUDAMED SRN
IT-MF-000029421