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A-scan probe 14130-0001

by Nidek Co., Ltd.

A-scan probe 14130-0001 is a Class II device made by Nidek Co., Ltd., listed in FDA GUDID since 10 Jul 2023 (UDI-DI 04987669200018), registry data as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04987669200018 UDI-DI Date10 Jul 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  • Withdrawn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
A-scan probe
Generic name
Ophthalmic ultrasound imaging system
Model / reference
14130-0001
Primary DI / UDI-DI
04987669200018
FDA product code
IYO
GMDN term
Ophthalmic ultrasound imaging system
Device class
Class II
Regulation number
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.

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See all devices from Nidek Co., Ltd. →

Properties

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