Skip to content

Frigitronics 2401

by CooperSurgical, Inc.

Frigitronics 2401 is a Class II device made by CooperSurgical, Inc., listed in FDA GUDID since 29 Jul 2016 (UDI-DI 00888937009583), 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 Number00888937009583 UDI-DI Date29 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  • Withdrawn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
Frigitronics
Generic name
General cryosurgical system, cryogen gas, mechanical
Model / reference
2401
Primary DI / UDI-DI
00888937009583
FDA product code
GEH
GMDN term
General cryosurgical system, cryogen gas, mechanical
Device class
Class II
Regulation number
878.4350
GUDID distribution status
In Commercial Distribution

Related devices

Category: General cryosurgical system, cryogen gas, mechanical

Similar devices

Other devices filed under FDA product code GEH (Unit, Cryosurgical, Accessories).

Other devices from CooperSurgical, Inc.

See all devices from CooperSurgical, Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Serial number
Other properties (12, all answered No)