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Easytech S.r.l.

Italy IT-MF-000017907 Last updated 8 Jun 2026

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Devices
15
Registries
EUDAMED
FDA recalls
0

Catalogue15

EUDAMED certificates1

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (1)

TUV Rheinland Italia SRL 1936 1 certificate

  • ITH 1343914 1 Amended

    Quality management system EU MDR

    Issued
    6 Oct 2025
    Expires
    19 Jul 2027
    Reason
    Other

Notified bodies

What Easytech S.r.l. makes

Easytech S.r.l. manufactures a range of orthopedic and rehabilitation devices, including knee braces (e.g., Genu ISO, Flextensor, Genu Plus), cryotherapy units (e.g., Cryo-T), and physiotherapy equipment (e.g., T Care Compact XP, T Care Plus). The portfolio also includes compression and support garments (e.g., Vector, Minivector) and orthopedic measurement tools (e.g., Prima ISO, T Dose).

The company’s devices are classified under EU Medical Device Regulations as Class I, Class IIa, and Class IIb, with all products 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 Easytech S.r.l. manufacture?

Easytech S.r.l. specializes in orthopedic and rehabilitation devices. Their portfolio includes knee braces like the Genu ISO and Flextensor, cryotherapy units such as the Cryo-T, physiotherapy equipment like the T Care Compact XP and T Care Plus, compression garments such as Vector and Minivector, and orthopedic measurement tools like the Prima ISO and T Dose. These devices are designed to support mobility, recovery, and therapeutic care.

Where is Easytech S.r.l. based, and how does that relate to their devices?

Easytech S.r.l. is headquartered in Italy. Being based in Italy aligns with the company’s compliance with EU Medical Device Regulations, ensuring their products meet the necessary standards for safety, performance, and regulatory requirements within the European market.

Which regulatory registries list Easytech S.r.l.’s devices?

All of Easytech S.r.l.’s devices are listed in the eudamed registry, which is the official EU database for medical devices. This registry ensures transparency and traceability of devices authorized under EU Medical Device Regulations, allowing healthcare professionals and regulators to verify product details.

How are Easytech S.r.l.’s devices classified under EU regulations?

Easytech S.r.l.’s devices fall under Class I, Class IIa, and Class IIb classifications under the EU Medical Device Regulations. The classification determines the level of scrutiny and regulatory requirements for each device, with Class IIa and IIb typically requiring additional risk assessments due to their higher potential risk to patients.

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

Information

Country
Italy
Address
32, Via della Fangosa, Borgo San Lorenzo , Italy
Phone
+39 055 8455216
PRRC contact
Stefano Manzo
EUDAMED SRN
IT-MF-000017907