Skip to content

Na DAQ916

by Medtronic Xomed, Inc. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00643169378476 UDI-DIDate1 May 2016ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Generic Name
Nerve-locating system
Model / Reference
DAQ916
Primary DI / UDI-DI
00643169378476
510(k) Number
FDA Product Code
GWF, GWQ, GWE, ITX, GWJ, IYN
GMDN Term
Nerve-locating system
Device Class
Class II
Regulation Number
882.1870, 882.1400, 882.1890, 892.1570, 882.1900, 892.1550
GUDID distribution status
In Commercial Distribution

Related devices

Category: Nerve-locating system

Cleared under the same submission (K061639)

Show all (12)

Other devices from Medtronic Xomed, Inc.

See all devices from Medtronic Xomed, Inc. →

Properties

  • Prescription Use
  • Serial 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
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No