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Reveal LINQ TM LNQ11

by Medtronic, Inc.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

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 Number00643169732216 UDI-DI Date14 May 2016ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Reveal LINQ TM
Generic Name
Implantable cardiac monitor
Model / Reference
LNQ11
Description
MON LNQ11 REVEAL LINQ USA RRT
Primary DI / UDI-DI
00643169732216
510(k) Number
FDA Product Code
DSI
GMDN Term
Implantable cardiac monitor
Device Class
Class II
Regulation Number
870.1025
GUDID distribution status
Not in Commercial Distribution
MRI Safety
MR Conditional

Other devices from Medtronic, Inc.

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Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Serial Number

Other properties (9)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No