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myLUX™ Patient App 622929-120

by Boston Scientific

Listed FDA GUDID listing, not in commercial distribution

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00802526623110 UDI-DI Date31 Aug 2023ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
myLUX™ Patient App
Generic Name
Implantable cardiac device management application software
Model / Ref / Catalog
622929-120, 2929
Primary DI / UDI-DI
00802526623110
FDA Product Code
MXD
GMDN Term
Implantable cardiac device management application software
Device Class
Class II
Regulation Number
870.1025
GUDID distribution status
Not in Commercial Distribution
MRI Safety
MR Unsafe

Other devices from Boston Scientific

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Properties

  • Prescription Use
  • Lot / Batch Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No