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Eli Ezer EUS-2600

by U.S. Ophthalmic, L.L.C.

Eli Ezer EUS-2600 is a Class II device made by U.S. Ophthalmic, L.L.C., listed in FDA GUDID since 17 Aug 2016 (UDI-DI 00851158007287), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00851158007287 UDI-DI Date17 Aug 2016ListedStatusListed 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  • Withdrawn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
Eli Ezer
Generic name
Ophthalmic ultrasound imaging system
Model / reference
EUS-2600
Primary DI / UDI-DI
00851158007287
FDA product code
ITX, IYO
GMDN term
Ophthalmic ultrasound imaging system
Device class
Class II
Regulation number
892.1570, 892.1560
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ophthalmic ultrasound imaging system

Similar devices in this category

Other devices filed under Ophthalmic ultrasound imaging system.

Other devices from U.S. Ophthalmic, L.L.C.

See all devices from U.S. Ophthalmic, L.L.C. →

Properties

  • Serial number
Other properties (14, all answered No)