Data / Medical devices / Set, I.V. Fluid Transfer / Italy
FDA-registered makers of Set, I.V. Fluid Transfer in Italy: 6 establishments
6 establishments in Italy are registered with the FDA to make Set, I.V. Fluid Transfer (product code LHI). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Set, I.V. Fluid Transfer
- Product code
- LHI
- Country
- Italy
Makers of Set, I.V. Fluid Transfer in Italy
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Aea SRL | Angeli di Rosora Ancona, Italy | Complaint file establishment, Specification developer | 1 | September 27, 2021 | 0 | 0 | 0 | api.fda.gov |
| B. Braun Avitum Italy S.p.A. | MIRANDOLA Modena, Italy | Contract manufacturer, Manufacturer | 1 | December 2, 2015 | 0 | 0 | 0 | api.fda.gov |
| Adria.med. SRL | Tocco Da Casauria Pescara, Italy | Contract manufacturer, Contract sterilizer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GVS SPA | Mirandola Modena, Italy | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GVS SPA | Borgocarbonara Mantova, Italy | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Industrie Borla, S.P.A. | Moncalieri Torino, Italy | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.