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Valleylab™ E15624

by Aspen Surgical Products, Inc. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10840113243034 UDI-DIDate18 Sep 2026ListedStatusListed 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  • Withdrawn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 23 Oct 2026.

Specification

GUDID

Trade Name
Valleylab™
Generic Name
Open-surgery electrosurgical electrode, monopolar, single-use
Model / Reference
E15624
Primary DI / UDI-DI
10840113243034
FDA Product Code
HGI
GMDN Term
Open-surgery electrosurgical electrode, monopolar, single-use
Device Class
Class II
Regulation Number
884.4120
GUDID distribution status
In Commercial Distribution

Other devices from Aspen Surgical Products, Inc.

See all devices from Aspen Surgical Products, Inc. →

Properties

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

Other properties (8)

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