Skip to content

Na MN13650

by Advanced Neuromodulation Systems

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 Number05415067053060 UDI-DI Date7 Dec 2025ListedStatusListed 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  • Withdrawn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
Neurosurgical procedure kit, non-medicated, single-use
Model / Ref / Catalog
MN13650
Primary DI / UDI-DI
05415067053060
PMA Number
FDA Product Code
PMP
GMDN Term
Neurosurgical procedure kit, non-medicated, single-use
Device Class
Class III
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe
Size
Length — 22.0000 Centimeter

Related devices

Cleared under the same submission (P150004)

Show all (12)

Other devices from Advanced Neuromodulation Systems

See all devices from Advanced Neuromodulation Systems →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Serial Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Manufacturing Date: No