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APIS Technologies

Switzerland CH-MF-000039694 Last updated 21 Oct 2026

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Devices
13
Registries
EUDAMEDGUDID
FDA recalls
0

Catalogue13

  • I-Stop Toms Ref IS-TOMS-4

    Class IIb EUDAMED Active

  • I-Stop Ref IS-1-A

    Class IIb EUDAMEDFDA UDI Active

  • I-Stop Ref IS-5

    Class IIb EUDAMEDFDA UDI Active

  • I-Stop Toms Ref IS-TOMS-1

    Class IIb EUDAMEDFDA UDI Active

  • I-Stop Toms Ref IS-TOMS-6

    Class IIb EUDAMED Active

  • I-Stop Ref IS-13

    Class IIb EUDAMED Active

  • I-Stop Ref IS-M-1

    Class IIb EUDAMEDFDA UDI Active

  • I-Stop Ref IS-6

    Class IIb EUDAMEDFDA UDI Active

  • I-Stop Ref IS-HELICO-01

    Class IIb EUDAMED Active

  • Pelvi-Stop Ref P-STOP-8

    Class IIb EUDAMED Active

  • Pelvi-Stop Ref P-STOP-20

    Class IIb EUDAMED Active

  • I-Stop Ref IS-10

    Class IIb EUDAMEDFDA UDI Active

  • Pelvi-Stop Ref P-STOP-4

    Class IIb EUDAMED Active

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Authorised representatives

About

APIS Technologies distributor, Swiss manufacturer of medical devices, specialized in uro-gynaecology for the treatment of urinary stress incontinence and prolapsus

Translated from the manufacturer's own website. Source

What APIS Technologies makes

APIS Technologies manufactures medical devices primarily for uro-gynaecology, including the I-STOP and PELVI-STOP systems. These products are designed to treat urinary stress incontinence and pelvic organ prolapse, offering solutions for surgical and minimally invasive procedures in these conditions.

The company’s devices fall under EU Class IIb classification and are listed in the EU’s eudamed registry. APIS Technologies operates as a Swiss manufacturer and distributor, adhering to European medical device regulations.

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 APIS Technologies manufacture?

APIS Technologies specializes in uro-gynaecology devices. Its portfolio includes the I-STOP and PELVI-STOP systems, which are designed for surgical and minimally invasive treatments of urinary stress incontinence and pelvic organ prolapse. These devices are tailored to address specific clinical needs in these areas.

Where is APIS Technologies based, and what is its role in the medical device industry?

APIS Technologies is based in Switzerland and operates as both a manufacturer and distributor of medical devices. As a Swiss manufacturer, it develops and produces its own products while also distributing them to healthcare providers, ensuring compliance with European medical device regulations throughout the process.

Which regulatory registries list APIS Technologies’ devices?

APIS Technologies’ devices are listed in the eudamed registry, which is the official European database for medical devices. This registry ensures transparency and traceability of devices authorized under EU regulations, including those classified under Class IIb.

How are APIS Technologies’ devices classified under EU regulations?

APIS Technologies’ devices fall under EU Class IIb classification. This classification is assigned based on risk assessment criteria—Class IIb devices pose moderate to high risks and require additional scrutiny, including conformity assessment procedures, to ensure their safety and performance before authorization.

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

Information

Country
Switzerland
Address
1, Rue de la Cité, Geneva, Switzerland
Phone
+41791041428(from company website)
PRRC contact
Vincent GORIA
EUDAMED SRN
CH-MF-000039694