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C.M.P. Cable W91218

by C.M.P. Canadian Medical Products Inc

C.M.P. Cable W91218 is a Class II device made by C.M.P. Canadian Medical Products Inc, listed in FDA GUDID since 16 Nov 2016 (UDI-DI B312W912180), 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 NumberB312W912180 UDI-DI Date16 Nov 2016ListedStatusListed 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  • Withdrawn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
C.M.P. Cable
Generic name
Transcutaneous electrical stimulation lead
Model / reference
W91218
Primary DI / UDI-DI
B312W912180
FDA product code
IKD
GMDN term
Transcutaneous electrical stimulation lead
Device class
Class II
Regulation number
890.1175
GUDID distribution status
In Commercial Distribution

Related devices

Category: Transcutaneous electrical stimulation lead

Similar devices

Other devices filed under FDA product code IKD (Cable, Electrode).

Other devices from Canadian Medical Products

See all devices from Canadian Medical Products →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)