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Chattanooga 47336

by Djo, LLC

Chattanooga 47336 is a Class II device made by Djo, LLC, listed in FDA GUDID since 27 Oct 2023 (UDI-DI 00190446750628), 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 Number00190446750628 UDI-DI Date27 Oct 2023ListedStatusListed 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  • Withdrawn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
Chattanooga
Generic name
Physical therapy ultrasound system applicator, hand-held
Model / reference
47336
Primary DI / UDI-DI
00190446750628
FDA product code
IMG
GMDN term
Physical therapy ultrasound system applicator, hand-held
Device class
Class II
Regulation number
890.5860
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code IMG (Stimulator, ultrasound and muscle, for use in applying therapeutic deep heat).

Other devices from Djo, LLC

See all devices from Djo, LLC →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)