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A902

by Medtronic, Inc.

A902 is a Class I device made by Medtronic, Inc., listed in FDA GUDID since 7 Sep 2017 (UDI-DI 00643169738065), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00643169738065 UDI-DI Date7 Sep 2017ListedStatusListed 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  • Withdrawn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
A902
Primary DI / UDI-DI
00643169738065
FDA product code
OUG
GMDN term
Multiple active implantable device programmer
Device class
Class I
Regulation number
880.6310
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
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)