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TM90P01

by Medtronic, Inc. 2 variants

TM90P01 is a Class III device made by Medtronic, Inc., listed in FDA GUDID since 5 Sep 2025 (UDI-DI 00763000269548), registry data as of 23 Oct 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00763000269548 UDI-DI Date5 Sep 2025ListedStatusListed 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  • Withdrawn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

Generic name
Multiple active implantable device programmer
Model / reference
TM90P01
Primary DI / UDI-DI
00763000269548
FDA product code
EZW
GMDN term
Multiple active implantable device programmer
Device class
Class III
Regulation number
876.5270
GUDID distribution status
In Commercial Distribution

Related devices

Category: Multiple active implantable device programmer

Similar devices in this category

Other devices filed under Multiple active implantable device programmer.

Other devices from Medtronic, Inc.

See all devices from Medtronic, Inc. →

Properties

  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Serial number
Other properties (11, all answered No)