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Capsure®sp Novus 5092-52

by Medtronic, Inc. GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00643169590670 UDI-DIDate14 Jan 2016ListedStatusListed GUDID: not 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  • Withdrawn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

Trade Name
Capsure®sp Novus
Generic Name
Endocardial/interventricular septal pacing lead
Model / Reference
5092-52
Primary DI / UDI-DI
00643169590670
PMA Number
FDA Product Code
NVN, NVY, DTB
GMDN Term
Endocardial/interventricular septal pacing lead
Device Class
Class III
Regulation Number
870.3680
GUDID distribution status
Not in Commercial Distribution
Size
Length — 52.0 Centimeter

Related devices

Cleared under the same submission (P850089)

Show all (12)

Other devices from Medtronic, Inc.

See all devices from Medtronic, Inc. →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Combination Product
  • Serial Number

Other properties (8)

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