Data / Medical devices / Warmer, Thermal, Infusion Fluid / Netherlands
FDA-registered makers of Warmer, Thermal, Infusion Fluid in the Netherlands: 6 establishments
6 establishments in the Netherlands are registered with the FDA to make Warmer, Thermal, Infusion Fluid (product code LGZ). 2 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
- Warmer, Thermal, Infusion Fluid
- Product code
- LGZ
- Country
- Netherlands
Makers of Warmer, Thermal, Infusion Fluid in the Netherlands
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| TSC Life | Almelo Overijssel, Netherlands | Manufacturer | 2 | November 18, 2025 | 0 | 0 | 0 | api.fda.gov |
| The Surgical Company International B.V. | Amsterdam Noord-Holland, Netherlands | Specification developer | 2 | November 18, 2025 | 0 | 0 | 0 | api.fda.gov |
| Aim B.V. | Brunssum Limburg, Netherlands | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ecm Europe BV | Gemert Noord-Brabant, Netherlands | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Unitron Group BV | IJzendijke Zeeland, Netherlands | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Variass Medical Systems BV | Drachten Fryslan, Netherlands | 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.