VisuALL VRP ETS VisuALL VRP ETS

GUDID 00860008686015

VisuALL VRP ETS

Olleyes, Inc.

Perimeter, automatic
Primary Device ID00860008686015
NIH Device Record Keyed6dc3ef-acd0-4d31-888d-32010bae0f5c
Commercial Distribution StatusIn Commercial Distribution
Brand NameVisuALL VRP ETS
Version Model Number1
Catalog NumberVisuALL VRP ETS
Company DUNS081297690
Company NameOlleyes, Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone999-999-9999
Emailinfo@olleyes.com
Phone999-999-9999
Emailinfo@olleyes.com
Phone999-999-9999
Emailinfo@olleyes.com
Phone999-999-9999
Emailinfo@olleyes.com
Phone999-999-9999
Emailinfo@olleyes.com
Phone999-999-9999
Emailinfo@olleyes.com
Phone999-999-9999
Emailinfo@olleyes.com
Phone999-999-9999
Emailinfo@olleyes.com
Phone999-999-9999
Emailinfo@olleyes.com
Phone999-999-9999
Emailinfo@olleyes.com
Phone999-999-9999
Emailinfo@olleyes.com
Phone999-999-9999
Emailinfo@olleyes.com
Phone999-999-9999
Emailinfo@olleyes.com
Phone999-999-9999
Emailinfo@olleyes.com
Phone999-999-9999
Emailinfo@olleyes.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100860008686015 [Primary]

FDA Product Code

HPTPerimeter, Automatic, Ac-Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-05-04
Device Publish Date2023-04-26

Devices Manufactured by Olleyes, Inc.

00860008686015 - VisuALL VRP ETS2023-05-04VisuALL VRP ETS
00860008686015 - VisuALL VRP ETS2023-05-04 VisuALL VRP ETS
00860008686022 - VisuALL VRP S2023-05-04 VisuALL VRP S

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.