Biosig Technologies
Country not established
Biosig Technologies is a medical device manufacturer, with 15 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 13 Nov 2026.
- Devices
- 15
Registry facts
- Registries
- FDA GUDID 14
- FDA 510(k) 1
- Device classes
- FDA Class II 15
What Biosig Technologies makes
Biosig Technologies manufactures components and systems for cardiac electrophysiology analysis, including jumper cables, catheter input modules, ECG cables, and splitter boxes designed for electrophysiological studies.
The company’s products are classified as Class II devices and are listed under FDA 510(k) and UDI registries.
Catalogue
Search and filter all 15 devicesFrequently asked questions
How many devices does Biosig Technologies have in the registry?
The registry currently lists 15 devices for Biosig Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biosig Technologies's devices?
Among its 15 most recently registered devices, Biosig Technologies has devices listed in FDA 510(k) (1 device) and FDA GUDID (14 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Biosig Technologies's devices fall under?
Among its 15 most recently registered devices, the classes recorded for Biosig Technologies's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biosig Technologies in the registry?
The most recently registered devices listed for Biosig Technologies include Pure EP - 5 x 4 pin Yoked Jumper Cable Red PE-002-016-005, Pure EP AE-0001-412, Pure EP - Catheter Input Module PE-002-007-000 and Pure EP - 5 x 10 pin Yoked Jumper Cable Blue PE-002-020-005.