Phasein AB
Country not established
- Devices
- 5
What Phasein AB makes
Phasein AB makes gas monitoring and analysis devices, including the VEO Multigas Monitor for Pocket PC, the EMMA Analyzer and Monitor in kPa and mmHg configurations, the IRMA CO2 Model 200101 and IRMA AX 200601, and the ISA CO2, ISA AX+, and ISA OR+ devices.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Veo Multigas Monitor For Pocket Pc Ref K081601
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Irma C02 Model 200101; Irma Ax 200601 Ref K123043
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Isa CO2, Isa Ax+, Isa Or+ Ref K103604
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Phasein AB have in the registry?
The registry currently lists 5 devices for Phasein AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Phasein AB's devices?
Among its 5 most recently registered devices, Phasein AB has devices listed in FDA 510(k) (5 devices).
What risk classes do Phasein AB's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Phasein AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Phasein AB in the registry?
The most recently registered devices listed for Phasein AB include VEO MULTIGAS MONITOR FOR POCKET PC, EMMA ANALYZER (KPA) AND (MMHG); EMMA MONITOR (KPA) AND (MMHG), IRMA C02 MODEL 200101; IRMA AX 200601 and EMMA ANALYZER (KPA & MMHG); EMMA MONITOR (KPA & MMHG).