Rite365 Premium W4

Rite365 Premium W4 is a Class II device made by Maybeam LLC, listed in FDA GUDID since 20 Dec 2018 (UDI-DI 00860000362320), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00860000362320 UDI-DI	Date20 Dec 2018Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00860000362320

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Rite365
Generic name: Patient monitoring system module, blood pressure, noninvasive
Model / reference: Premium W4

Primary DI / UDI-DI: 00860000362320
FDA product code: DXN
GMDN term: Patient monitoring system module, blood pressure, noninvasive

Device class: Class II
Regulation number: 870.1130
GUDID distribution status: In Commercial Distribution

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Properties

Lot / batch number
Manufacturing date

Other properties (13, all answered No)