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Quadrastim 9G0005

by Dynatronics Corp.

Quadrastim 9G0005 is a Class II device made by Dynatronics Corp., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10660584000406), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 Number10660584000406 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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
Quadrastim
Generic name
Transcutaneous electrical stimulation electrode, single-use
Model / reference
9G0005
Primary DI / UDI-DI
10660584000406
FDA product code
GXY
GMDN term
Transcutaneous electrical stimulation electrode, single-use
Device class
Class II
Regulation number
882.1320
GUDID distribution status
Not in Commercial Distribution
Size
Area/Surface Area — 3.6 Square inch

Similar devices

Other devices filed under FDA product code GXY (Electrode, Cutaneous).

Other devices from Dynatronics Corp.

See all devices from Dynatronics Corp. →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)