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Venusa, Ltd.

Country not established

Devices
8

What Venusa, Ltd. makes

Venusa, Ltd. manufactures intravenous (I.V.) administration sets, including bolus/infusion sets, extension sets with integrated filters, and Y-site connectors for multi-line infusions. Their portfolio also includes enteral feeding bags with attached tubing for nutritional delivery and specialized I.V. sets designed for fluid administration, such as the FLU VEN and FLU MET series. Needle-based infusion sets and pre-filled fluid containers complete the product range, catering to hospital and clinical infusion needs.

All listed devices fall under Class II regulatory classification in the US, requiring premarket notification (510(k)) clearance via the FDA. The company’s products are registered under the FDA 510(k) pathway, ensuring compliance with US medical device regulations. Venusa, Ltd. is headquartered in the United States.

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

Catalogue8

Newest first, rows 1-8 of 8

Frequently asked questions

How many devices does Venusa, Ltd. have in the registry?

The registry currently lists 8 devices for Venusa, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Venusa, Ltd.'s devices?

Among its 8 most recently registered devices, Venusa, Ltd. has devices listed in FDA 510(k) (8 devices).

What risk classes do Venusa, Ltd.'s devices fall under?

Among its 8 most recently registered devices, the classes recorded for Venusa, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Venusa, Ltd. in the registry?

The most recently registered devices listed for Venusa, Ltd. include FLU VEN I.V. SET 0153-C PERMA-SET, BERLEX BOLUS/INFUSION(TM) INTRAVENOUS ADMIN SET, ENTERAL FEEDING BAG, 1000 ML, & TUBING SET and FLU MET 2.

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