Data / Medical devices / Set, I.V. Fluid Transfer / Germany
FDA-registered makers of Set, I.V. Fluid Transfer in Germany: 5 establishments
5 establishments in Germany are registered with the FDA to make Set, I.V. Fluid Transfer (product code LHI). 3 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Set, I.V. Fluid Transfer
- Product code
- LHI
- Country
- Germany
Makers of Set, I.V. Fluid Transfer in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| SFM Medical Devices GmbH | Waechtersbach Hesse, Germany | Manufacturer | 3 | September 6, 2024 | 0 | 0 | 0 | api.fda.gov |
| B. Braun Melsungen AG | MELSUNGEN Hesse, Germany | Manufacturer, Specification developer | 2 | December 9, 2020 | 0 | 0 | 0 | api.fda.gov |
| Fresenius Kabi Deutschland GMBH | BAD HERSFELD Hesse, Germany | Specification developer | 1 | June 1, 2022 | 0 | 0 | 0 | api.fda.gov |
| RAUMEDIC - Muenchberg | Helmbrechts Bavaria, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Roechling Medical Waldachtal AG | Waldachtal Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.