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EchoBed EB723

by Medical Positioning, Inc.

EchoBed EB723 is a Class I device made by Medical Positioning, Inc., listed in FDA GUDID since 20 Apr 2026 (UDI-DI 00848871001500), 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 Number00848871001500 UDI-DI Date20 Apr 2026ListedStatusListed 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  • Withdrawn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
EchoBed
Generic name
Multi-purpose diagnostic imaging table
Model / reference
EB723
Primary DI / UDI-DI
00848871001500
FDA product code
LGX
GMDN term
Multi-purpose diagnostic imaging table
Device class
Class I
Regulation number
878.4960
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LGX (Table, Examination, Medical, Powered).

Other devices from Medical Positioning, Inc.

See all devices from Medical Positioning, Inc. →

Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)