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Na 6983

by Boston Scientific GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00802526489723 UDI-DIDate24 Sep 2014ListedStatusListed 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  • Withdrawn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
Pacing/defibrillation lead stylet
Model / Reference
6983
Primary DI / UDI-DI
00802526489723
PMA Number
FDA Product Code
LWP
GMDN Term
Pacing/defibrillation lead stylet
Device Class
Class III
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pacing/defibrillation lead stylet

Cleared under the same submission (P830060)

Show all (10)

Other devices from Boston Scientific

See all devices from Boston Scientific →

Properties

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