N/A 9731965

by Medtronic Navigation, Inc. 2 variants

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

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

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00885074328195 UDI-DI	Date18 Jun 2016Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name: Stereotactic surgery system probe, reusable
Model / Reference: 9731965

Primary DI / UDI-DI: 00885074328195
FDA Product Code: HAW
GMDN Term: Stereotactic surgery system probe, reusable

Device Class: Class II
Regulation Number: 882.4560
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

Size: Outer Diameter — 4.3 Millimeter

Other devices from Medtronic Navigation, Inc.

Autoguide Surgical Instruments

Class I
IPC Cart and IV Pole

Class I
Autoguide System

Class I
S8 Clinical Application Software

Class IIb
Registration Probe

Class I
Active Wireless Tracker

Class I

See all devices from Medtronic Navigation, Inc. →

Properties

Prescription Use
Lot / Batch Number

Other properties (12)

Sterile: No
Single Use: No
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