Somnostar 26322-001

No FDA recalls on record, checked 23 Oct 2026.

Trade Name

Somnostar

Generic Name

Home-use sleep apnoea recording system

Model / Ref / Catalog

26322-001

Primary DI / UDI-DI

10846446032208

FDA Product Code

OLV

GMDN Term

Home-use sleep apnoea recording system

Device Class

Class II

Regulation Number

882.1400

GUDID distribution status

Not in Commercial Distribution

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