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N/A 33TH69L

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 Number00763000810580 UDI-DI Date22 Apr 2024ListedStatusListed 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  • Withdrawn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

Generic Name
Deep brain electrical stimulation system
Model / Reference
33TH69L
Primary DI / UDI-DI
00763000810580
PMA Number
FDA Product Code
MRU
GMDN Term
Deep brain electrical stimulation system
Device Class
Unclassified
GUDID distribution status
In Commercial Distribution

Related devices

Category: Deep brain electrical stimulation system

Cleared under the same submission (H020007)

Show all (12)

Other devices from Medtronic, Inc.

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Properties

  • Implantable
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number

Other properties (10)

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