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Voyant Electrosurgical Generator EA030

by Applied Medical Resources Corp. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00607915146467 UDI-DIDate16 Jan 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  • Withdrawn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
Voyant Electrosurgical Generator
Generic Name
Electrosurgical system generator
Model / Reference
EA030
Primary DI / UDI-DI
00607915146467
FDA Product Code
GEI
GMDN Term
Electrosurgical system generator
Device Class
Class II
Regulation Number
878.4400
GUDID distribution status
In Commercial Distribution

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Properties

  • Prescription Use
  • Lot / Batch Number
  • Serial 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
  • Premarket Exempt: No
  • Expiration Date: No