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Erich Jaeger GmbH

Also registered as Erich Jaeger GmbH & Co. KG, Erich Jaeger, Inc.

Country not established

Devices
37

What Erich Jaeger GmbH makes

Erich Jaeger GmbH manufactures diagnostic devices for respiratory and sleep medicine, including cardiorespiratory monitoring systems like SLEEPSCREEN/APNOESCREEN CARDIO, spirometry equipment such as SPIRO PRO, and aerosol provocation systems like the APS PRO. Their portfolio also includes portable oxygen saturation monitors (OXYCON MOBILE) and pediatric respiratory measurement devices, such as the MS PAED-BABY BODY.

The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. Their products are intended for use in the United States, where regulatory compliance is required for market authorization.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue37

Newest first, rows 1-37 of 37

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  • Master Screen Pnuemo Ref K933839

    Class II
    Active 510(k) 510(k) II

  • Flowscreen Ref K932744

    Class II
    Active 510(k) 510(k) II

  • Sleepscreen/Apnoescreen Cardio Ref K021138

    Class II
    Active 510(k) 510(k) II

  • Lauf-Ergotest Ref K843853

    Class I
    Active 510(k) 510(k) I

  • Masterscreen Pft Body Ref K951901

    Class II
    Active 510(k) 510(k) II

  • Universal-Ergotest Ref K843850

    Class II
    Active 510(k) 510(k) II

  • Pneumoscope Ref K852337

    Class II
    Active 510(k) 510(k) II

  • Apta-Bronchoscreen Ref K843852

    Class II
    Active 510(k) 510(k) II

  • Infant Body Test Ref K853390

    Class II
    Active 510(k) 510(k) II

  • Masterscreen Ios Ref K954140

    Class II
    Active 510(k) 510(k) II

  • Spiro Pro Ref K000648

    Class II
    Active 510(k) 510(k) II

  • Alveo-Diffusion Test Ref K853443

    Class II
    Active 510(k) 510(k) II

  • Ergo-Pneumotest Ref K853434

    Class II
    Active 510(k) 510(k) II

  • Pneumoscreen Ref K843849

    Class II
    Active 510(k) 510(k) II

  • Asthma Monitor AM2 Ref K980876

    Class II
    Active 510(k) 510(k) II

  • Transferscreen Ii Ref K843857

    Not classified
    Active 510(k) 510(k) —

  • Bodyscreen Ii Ref K843851

    Class II
    Active 510(k) 510(k) II

  • Universal-Bodytest Ref K843846

    Class II
    Active 510(k) 510(k) II

  • Lauf-Ergotest Junior Ref K843859

    Class I
    Active 510(k) 510(k) I

  • Oxyscreen Ref K843860

    Class II
    Active 510(k) 510(k) II

  • Aerosol Provocation System Aps Pro, Model Aps Pro Ref K001502

    Class II
    Active 510(k) 510(k) II

  • N20 Test Ref K853360

    Class II
    Active 510(k) 510(k) II

  • Apnoescreen Pro, Alpha Screen Pro Ref K000396

    Class II
    Active 510(k) 510(k) II

  • Screenmate Ref K853409

    Class II
    Active 510(k) 510(k) II

  • N2 Test Ref K843840

    Not classified
    Active 510(k) 510(k) —

  • Masterscreen Body Ref K936108

    Class II
    Active 510(k) 510(k) II

  • Co Test Ref K843845

    Class II
    Active 510(k) 510(k) II

  • CO2 Test Ref K843844

    Class II
    Active 510(k) 510(k) II

  • Ergotest 40 & 45 Ref K843855

    Class I
    Active 510(k) 510(k) I

  • Toennies Neuroscreen System Ref K972419

    Class II
    Active 510(k) 510(k) II

  • Oxycon Mobile Ref K023120

    Class II
    Active 510(k) 510(k) II

  • Ergo-Oxyscreen Ref K843841

    Class II
    Active 510(k) 510(k) II

  • O2 Test Ref K843847

    Class II
    Active 510(k) 510(k) II

  • He Test Ref K843843

    Class II
    Active 510(k) 510(k) II

  • Asthma Monitor Ref K960078

    Class II
    Active 510(k) 510(k) II

  • Aw Test Ref K843848

    Class II
    Active 510(k) 510(k) II

  • Ms Paed-Baby Body Ref K023796

    Class II
    Active 510(k) 510(k) II

Rows 1-37 of 37

Frequently asked questions

How many devices does Erich Jaeger GmbH have in the registry?

The registry currently lists 37 devices for Erich Jaeger GmbH. Devices recorded under merged duplicate company entries are counted once.

Which registries list Erich Jaeger GmbH's devices?

Among its 37 most recently registered devices, Erich Jaeger GmbH has devices listed in FDA 510(k) (37 devices).

What risk classes do Erich Jaeger GmbH's devices fall under?

Among its 37 most recently registered devices, the classes recorded for Erich Jaeger GmbH's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Erich Jaeger GmbH in the registry?

The most recently registered devices listed for Erich Jaeger GmbH include MASTER SCREEN PNUEMO, FLOWSCREEN, SLEEPSCREEN/APNOESCREEN CARDIO and LAUF-ERGOTEST.

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