Med2000 S.r.l.
Country not established
- Devices
- 3
What Med2000 S.r.l. makes
Med2000 S.R.L. manufactures nebulizer compressor devices, including standalone compressors paired with nebulizers (models P1, P2, P3, P4, P5) and standalone nebulizers with integrated accessories (e.g., the AndyFlow model A1/C). These devices are designed for respiratory therapy to deliver aerosolized medication.
The company’s products fall under FDA Class II medical devices and are listed via 510(k) clearance in the United States. The portfolio is regulated under US FDA requirements, with no additional European or international listings referenced.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Med2000 S.R.L. have in the registry?
The registry currently lists 3 devices for Med2000 S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Med2000 S.R.L.'s devices?
Among its 3 most recently registered devices, Med2000 S.R.L. has devices listed in FDA 510(k) (3 devices).
What risk classes do Med2000 S.R.L.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Med2000 S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Med2000 S.R.L. in the registry?
The most recently registered devices listed for Med2000 S.R.L. include MED2000 SPA NEBULIZER COMPRESSORS, MODELS P1 AND P2, WITH NEBULIZER, AND MED2000 SPA NEBULIZER, MODEL A1/C (ANDYFLOW), MED2000 SPA NEBULIZER ANDYFLOW, MODEL A1/C WITH ACCESSORIES and MED2000 NEBULIZER COMPRESSOR, MODELS P3, P4, P5 WITH NEBULIZER.