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Ecco 102436

by B. Ali Impex

Ecco 102436 is a Class I device made by B. Ali Impex, listed in FDA GUDID since 29 Jan 2024 (UDI-DI 08964003163587), 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 Number08964003163587 UDI-DI Date29 Jan 2024ListedStatusListed 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  • Withdrawn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
Ecco
Generic name
Dental articulator
Model / reference
102436
Primary DI / UDI-DI
08964003163587
FDA product code
EJP
GMDN term
Dental articulator
Device class
Class I
Regulation number
872.3150
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code EJP (Articulators).

Other devices from B. Ali Impex

See all devices from B. Ali Impex →

Properties

  • Sterilise before use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)