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Stealth AXiS 9736517

by Medtronic Navigation, Inc. United States GUDID

Product code HAW

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00763000928896 UDI-DIDate11 Apr 2026ListedStatusIn distribution

Coverage

1 jurisdiction

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  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls: none on record (FDA, checked 23 Oct 2026)

Specification

GUDID · synced 23 Oct 2026

Trade Name
Stealth AXiS
Generic Name
Multi-purpose stereotactic surgery system
Model / Reference
9736517
Primary DI / UDI-DI
00763000928896
510(k) Number
FDA Product Code
HAW
GMDN Term
Multi-purpose stereotactic surgery system
Device Class
Class II
Regulation Number
882.4560
Commercial Distribution
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

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Properties & raw data

Show properties, registry sources and raw records
  • Lot / Batch Number
Other properties (13)
  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: 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

Sources (1)

  • FDA UDI 326ee2d3-5651-4bc9-8f28-5dc9fd29310a 35 fields · synced 23 Oct 2026