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Na MDP201

by Medtronic Xomed, Inc. 3 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

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00763000242770 UDI-DIDate4 Jul 2019ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Nerve-locating system
Model / Reference
MDP201
Primary DI / UDI-DI
00763000242770
510(k) Number
FDA Product Code
GWJ, GWQ, IYN, GWE, GWF, ITX
GMDN Term
Nerve-locating system
Device Class
Class II
Regulation Number
882.1900, 882.1400, 892.1550, 882.1890, 882.1870, 892.1570
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