Skip to content

Evoke® CAP24 Paddle Lead Kit 3053

by Saluda Medical Pty Limited

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 Number09352307001756 UDI-DI Date6 Jul 2026ListedStatusListed 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  • Withdrawn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

Trade Name
Evoke® CAP24 Paddle Lead Kit
Generic Name
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection
Model / Reference
3053
Primary DI / UDI-DI
09352307001756
PMA Number
FDA Product Code
LGW, QRB
GMDN Term
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection
Device Class
Class III
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional
Size
Length — 70 Centimeter

Related devices

Cleared under the same submission (P190002)

Show all (12)

Other devices from Saluda Medical Pty Limited

See all devices from Saluda Medical Pty Limited →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No