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Valleylab E3530-3

by Covidien LP

Valleylab E3530-3 is a Class II device made by Covidien LP, listed in FDA GUDID since 7 May 2020 (UDI-DI 10884521767904), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10884521767904 UDI-DI Date7 May 2020ListedStatusListed GUDID: in commercial distribution

Official records

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  • Withdrawn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
Inert gas-enhanced endoscopic electrosurgical electrode, single-use
Model / reference
E3530-3
Primary DI / UDI-DI
10884521767904
FDA product code
GEI
GMDN term
Inert gas-enhanced endoscopic electrosurgical electrode, single-use
Device class
Class II
Regulation number
878.4400
GUDID distribution status
In Commercial Distribution
Size
Length — 3 Inch

Related devices

Category: Inert gas-enhanced endoscopic electrosurgical electrode, single-use

Similar devices in this category

Other devices filed under Inert gas-enhanced endoscopic electrosurgical electrode, single-use.

Other devices from Covidien LP

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    Class II

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  • Shiley 110865

    Class II

  • Shiley 110870

    Class II

See all devices from Covidien LP →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
Other properties (11, all answered No)