Skip to content

Cameron-Miller 26-2025

by Cameron-Miller, Inc.

Cameron-Miller 26-2025 is a Class II device made by Cameron-Miller, Inc., listed in FDA GUDID since 11 Feb 2017 (UDI-DI B3702620250), 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 NumberB3702620250 UDI-DI Date11 Feb 2017ListedStatusListed 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  • Withdrawn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
Cameron-Miller
Generic name
Electrosurgical handpiece, reusable
Model / reference
26-2025
Primary DI / UDI-DI
B3702620250
FDA product code
GEI
GMDN term
Electrosurgical handpiece, reusable
Device class
Class II
Regulation number
878.4400
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electrosurgical handpiece, reusable

Similar devices in this category

Other devices filed under Electrosurgical handpiece, reusable.

Other devices from Cameron-Miller, Inc.

See all devices from Cameron-Miller, Inc. →

Properties

  • Premarket exempt
Other properties (14, all answered No)