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Argus ll Psychophysical Test System 014202-002-R

by Second Sight Medical Products, Inc.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00856264005417 UDI-DI Date6 May 2015ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Argus ll Psychophysical Test System
Generic Name
Retinal prosthesis system tester/clinical evaluator
Model / Ref / Catalog
014202-002-R, 014202
Description
Laptop computer that is connected to the Clinician Programming System. It can be used to run performance evaluation software.
Primary DI / UDI-DI
00856264005417
PMA Number
FDA Product Code
NBF
GMDN Term
Retinal prosthesis system tester/clinical evaluator
Device Class
Unclassified
GUDID distribution status
Not in Commercial Distribution

Properties

  • Prescription Use
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No