Lifewatch
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Lifewatch is a medical device manufacturer, with 11 devices listed in FDA GUDID (FDA Class II) as of 13 Nov 2026.
- Devices
- 11
Registry facts
- Registries
- FDA GUDID 11
- Device classes
- FDA Class II 11
- Identifiers
- DUNS 797936734
What Lifewatch makes
Lifewatch manufactures electrocardiography (ECG) telemetric monitoring systems, including wearable transmitters for continuous cardiac rhythm monitoring. Devices include mobile cardiac telemetry systems with 1-lead and 3-lead configurations, as well as specialized transmitters for atrial fibrillation detection and patch-based monitoring.
The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database.
Catalogue
Search and filter all 11 devicesCompany details
- DUNS number
- 797936734
- Phone
- 1-800-700-3788
Frequently asked questions
How many devices does Lifewatch have in the registry?
The registry currently lists 11 devices for Lifewatch. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lifewatch's devices?
Among its 11 most recently registered devices, Lifewatch has devices listed in FDA GUDID (11 devices).
What risk classes do Lifewatch's devices fall under?
Among its 11 most recently registered devices, the classes recorded for Lifewatch's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lifewatch in the registry?
The most recently registered devices listed for Lifewatch include Explorer, LifeWatch Mobile Cardiac Telemetry 3-Lead MCT 3L-Brigadier-Verizon, MicroER and King of Hearts AF.