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VERSAN & DAFNE M.D. SRL

Italy·IT-PR-000047684

Last updated May 23, 2026

What VERSAN & DAFNE M.D. SRL makes

Versan & Dafne M.D. Srl manufactures kits for medical nebulization, including filler kits, nebulizer kits, and the PIPAC kit. These products are designed for respiratory therapy and localized drug delivery, supporting procedures such as aerosolized medication administration and pressurized intratumoral aerosol chemotherapy (PIPAC).

The company’s portfolio includes devices classified as Class IIa and Class IIb under EU regulations, all of which are registered in the EUDAMED database. 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 Versan & Dafne M.D. Srl manufacture?

Versan & Dafne M.D. Srl specializes in manufacturing kits for medical nebulization. Their portfolio includes kits like filler kits, nebulizer kits, and the PIPAC kit, which are primarily used for respiratory therapy and localized drug delivery. These devices support procedures such as aerosolized medication administration and pressurized intratumoral aerosol chemotherapy (PIPAC).

Where is Versan & Dafne M.D. Srl based?

Versan & Dafne M.D. Srl is based in Italy. The company’s location is relevant for understanding its regulatory framework and compliance with European Union medical device standards.

Which regulatory registries list the devices manufactured by Versan & Dafne M.D. Srl?

The devices produced by Versan & Dafne M.D. Srl are registered in the EUDAMED database, which is the European Union’s medical device registry. This database is used to track and monitor medical devices that have undergone the necessary regulatory processes under EU regulations.

How are the devices manufactured by Versan & Dafne M.D. Srl classified under EU regulations?

The devices manufactured by Versan & Dafne M.D. Srl fall into Class IIa and Class IIb classifications under EU medical device regulations. These classifications are determined based on the risk associated with the device, with Class IIa representing moderate risk and Class IIb representing higher risk, requiring additional scrutiny and compliance measures.

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

Information

Country
Italy
Address
25, VIALE ARCHIMEDE, ZEVIO, Italy
LinkedIn
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Facebook
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Phone
+39 045569949
PRRC Contact
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EUDAMED SRN
IT-PR-000047684
FDA FEI Number
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DUNS Number
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Catalogue (5)

DeviceModel / ReferenceRegistriesClassStatus
Kit Filler VD2
EUDAMED
Class IIaActive
Kit Nebulizzatore VDPP04
EUDAMED
Class IIaActive
Kit Nebulizzatore VDPP03
EUDAMED
Class IIbActive
Kit Pipac VDPIPAC-003L
EUDAMED
Class IIbActive
Kit Filler Evo VD1
EUDAMED
Class IIaActive

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