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Unomedical Devices S.A DE C.V.

MexicoFDA 510(k) applicant, unverified FDA

Devices
1
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

What Unomedical Devices S.A DE C.V. makes

Unomedical Devices S.A de C.V. manufactures the NERIA Multi Subcutaneous Infusion Set, a device designed for continuous or intermittent subcutaneous infusion of fluids, including insulin or other medications.

The NERIA Multi Subcutaneous Infusion Set is classified as a Class II medical device in the U.S. and is listed under the FDA’s 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Unomedical Devices S.A de C.V Reynosa Tamaulipas · MX FEI 3003442380

Frequently asked questions

How many devices does Unomedical Devices S.A DE C.V. have in the registry?

The registry currently lists 1 device for Unomedical Devices S.A DE C.V.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Unomedical Devices S.A DE C.V.'s devices?

Among its 1 most recently registered device, Unomedical Devices S.A DE C.V. has devices listed in FDA 510(k) (1 device).

What risk classes do Unomedical Devices S.A DE C.V.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Unomedical Devices S.A DE C.V.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Unomedical Devices S.A DE C.V. in the registry?

The most recently registered devices listed for Unomedical Devices S.A DE C.V. include NERIA MULTI SUBCUTANEOUS INFUSION SET.

Which FDA establishments are linked to Unomedical Devices S.A DE C.V.?

1 FDA establishment is linked to Unomedical Devices S.A DE C.V. in the registry; they are listed on the company page.

Generated automatically from registry data and not verified by a human reviewer.