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Elmed 5807-05

by Elmed Incorporated

Elmed 5807-05 is a Class II device made by Elmed Incorporated, listed in FDA GUDID since 21 Jul 2016 (UDI-DI 00842180104150), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00842180104150 UDI-DI Date21 Jul 2016ListedStatusListed 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  • Withdrawn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
Elmed
Generic name
Open-surgery electrosurgical electrode, monopolar, reusable
Model / Ref / Catalog
5807-05
Primary DI / UDI-DI
00842180104150
FDA product code
GEI
GMDN term
Open-surgery electrosurgical electrode, monopolar, reusable
Device class
Class II
Regulation number
878.4400
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Open-surgery electrosurgical electrode, monopolar, reusable

Other devices from Elmed Incorporated

See all devices from Elmed Incorporated →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Manufacturing date
Other properties (11, all answered No)