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Cameron-Miller 26-1230

by Cameron-Miller, Inc.

Cameron-Miller 26-1230 is a Class II device made by Cameron-Miller, Inc., listed in FDA GUDID since 11 Feb 2017 (UDI-DI B3702612300), 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 NumberB3702612300 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  • Withdrawn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
Open-surgery electrosurgical electrode, monopolar, reusable
Model / reference
26-1230
Primary DI / UDI-DI
B3702612300
FDA product code
JOS
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 Cameron-Miller, Inc.

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Properties

  • Sterilise before use
  • Premarket exempt
Other properties (13, all answered No)