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Symphion Operative Hysteroscopy System Prime Controller FG-PRIME25

by Minerva Surgical, Inc.

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850033976335 UDI-DI Date31 Oct 2025ListedStatusListed 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  • Withdrawn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
Symphion Operative Hysteroscopy System Prime Controller
Generic Name
Electrolytic-plasma electrosurgical system
Model / Ref / Catalog
FG-PRIME25
Primary DI / UDI-DI
00850033976335
FDA Product Code
HIG, PGT
GMDN Term
Electrolytic-plasma electrosurgical system
Device Class
Class II
Regulation Number
884.1700, 884.1710
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Other devices from Minerva Surgical, Inc.

See all devices from Minerva Surgical, Inc. →

Properties

  • Prescription Use
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • 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
  • Lot / Batch Number: No
  • Expiration Date: No