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Liberant™ LMT-CTRX

by Medtronic, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00763000998011 UDI-DI Date9 May 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Liberant™
Generic Name
Thrombectomy suction catheter
Model / Reference
LMT-CTRX
Primary DI / UDI-DI
00763000998011
510(k) Number
FDA Product Code
KRA, QEZ
GMDN Term
Thrombectomy suction catheter
Device Class
Class II
Regulation Number
870.1210, 870.5150
GUDID distribution status
In Commercial Distribution
Size
Guidewire Diameter — 0.36 Millimeter
Length — 140.0 Centimeter
Guidewire Compatibility — 6.0 French
Catheter Inner Diameter — 1.78 Millimeter

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number

Other properties (10)

  • 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