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Medix Medical Electronics (U.S.A.), Inc.

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Devices
14

What Medix Medical Electronics (U.S.A.), Inc. makes

Medix Medical Electronics manufactures respiratory and infusion monitoring devices, including ventilator monitoring systems like the VENTI-MONITOR Model 101, spirometers for lung function testing, and oxygen controllers for precise gas delivery. Their product line also covers insulin pumps such as the INSUMAT 229, syringe drivers for precise medication delivery, and apnea monitors for neonatal care. Temperature and tidal volume monitors complete the portfolio for patient vital sign tracking.

All listed devices fall under Class II regulatory classification in the U.S. and are recorded in the FDA 510(k) Premarket Notification database. The company operates under U.S. jurisdiction, adhering to domestic medical device regulations.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue14

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  • Venti-Monitor Model 101 Ref K812041

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Spirometer 210/211 Ref K812039

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Infusafe 205 Catolog No. 205.000 Ref K852433

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Syringe Driver 209 Ref K813562

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Infant Apnea Monitor Model 100 Ref K812045

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Oxygen Monitor 140/141 Ref K812040

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Oxygen Controller Model 145 Ref K812038

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Parenteral Infuser Medipump 204 Ref K861001

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Infusion Pump Model 200/201 Ref K812042

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Insulin Pump Insumat 229 Ref K853393

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Temperature Monitor 130/131/133 Ref K812037

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Tidal Volume Monitor 150 Ref K812046

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Respiration Rate Monitor 120/121 Ref K812044

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Enternal Infuser Multipump 203 Ref K861040

    Active Regimes: 510(k) Registry: 510(k) Class:II

Rows 1-14 of 14

Frequently asked questions

How many devices does Medix Medical Electronics (U.S.A.), Inc. have in the registry?

The registry currently lists 14 devices for Medix Medical Electronics (U.S.A.), Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Medix Medical Electronics (U.S.A.), Inc.'s devices?

Among its 14 most recently registered devices, Medix Medical Electronics (U.S.A.), Inc. has devices listed in FDA 510(k) (14 devices).

What risk classes do Medix Medical Electronics (U.S.A.), Inc.'s devices fall under?

Among its 14 most recently registered devices, the classes recorded for Medix Medical Electronics (U.S.A.), Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Medix Medical Electronics (U.S.A.), Inc. in the registry?

The most recently registered devices listed for Medix Medical Electronics (U.S.A.), Inc. include VENTI-MONITOR MODEL 101, SPIROMETER 210/211, INFUSAFE 205 CATOLOG NO. 205.000 and SYRINGE DRIVER 209.

Generated automatically from registry data and not verified by a human reviewer.