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STAR Artemis Mapping System

by Rhythm Ai Inc

STAR Artemis Mapping System is a Class II device made by Rhythm Ai Inc, listed in FDA GUDID since 26 Oct 2026 (UDI-DI 00860009793538), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860009793538 UDI-DI Date26 Oct 2026ListedStatusListed 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  • Withdrawn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
STAR Artemis
Generic name
Cardiac mapping system application software
Model / Ref / Catalog
STAR Artemis Mapping System
Primary DI / UDI-DI
00860009793538
FDA product code
DQK
GMDN term
Cardiac mapping system application software
Device class
Class II
Regulation number
870.1425
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code DQK (Computer, Diagnostic, Programmable).

Other devices from Rhythm Ai Inc

Properties

  • Prescription use
  • Manufacturing date
Other properties (13, all answered No)