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Na Sl-C1005-20

by St. Jude Medical, Inc.

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 Number05415067028228 UDI-DI Date10 Apr 2017ListedStatusListed 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  • Withdrawn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
Percutaneous radio-frequency ablation probe cannula, single-use
Model / Ref / Catalog
SL-C1005-20
Primary DI / UDI-DI
05415067028228
FDA Product Code
GXI
GMDN Term
Percutaneous radio-frequency ablation probe cannula, single-use
Device Class
Class II
Regulation Number
882.4725
GUDID distribution status
In Commercial Distribution
Size
Length — 10 Centimeter
Needle Gauge — 20 Gauge

Related devices

Category: Percutaneous radio-frequency ablation probe cannula, single-use

Other devices from St. Jude Medical, Inc.

See all devices from St. Jude Medical, Inc. →

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