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Valleylab E1000

by Covidien LP

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 Number10884524003047 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Valleylab
Generic Name
Open-surgery electrosurgical electrode, monopolar, reusable
Model / Reference
E1000
Primary DI / UDI-DI
10884524003047
FDA Product Code
GEI, JOS
GMDN Term
Open-surgery electrosurgical electrode, monopolar, reusable
Device Class
Class II
Regulation Number
878.4400
GUDID distribution status
In Commercial Distribution
Sterilization Method
Ethylene Oxide
Size
Length — 3.2 Millimeter

Related devices

Category: Open-surgery electrosurgical electrode, monopolar, reusable

Other devices from Covidien LP

See all devices from Covidien LP →

Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No