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Rite365 CB 15

by Maybeam LLC

Rite365 CB 15 is a Class II device made by Maybeam LLC, listed in FDA GUDID since 30 Oct 2018 (UDI-DI 00860000362313), 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

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860000362313 UDI-DI Date30 Oct 2018ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Rite365
Generic name
Cardiopulmonary resuscitation kit, single-use
Model / reference
CB 15
Primary DI / UDI-DI
00860000362313
FDA product code
CBP
GMDN term
Cardiopulmonary resuscitation kit, single-use
Device class
Class II
Regulation number
868.5870
GUDID distribution status
In Commercial Distribution

Related devices

Category: Cardiopulmonary resuscitation kit, single-use

Similar devices

Other devices filed under FDA product code CBP (Valve, Non-Rebreathing).

Other devices from Maybeam LLC

Properties

  • Lot / batch number
  • Expiration date
Other properties (13, all answered No)