OCULUS Easyfield VR

GUDID 00850040295818

The Hilsinger Company Parent LLC

Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector Visual acuity projector
Primary Device ID00850040295818
NIH Device Record Keye7c2d914-b265-4a5f-a9d0-9bc86ec4b627
Commercial Distribution StatusIn Commercial Distribution
Brand NameOCULUS Easyfield VR
Version Model NumberOCVR-01
Company DUNS118021111
Company NameThe Hilsinger Company Parent LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone8882848004
Emailservice@oculususa.com
Phone8882848004
Emailservice@oculususa.com
Phone8882848004
Emailservice@oculususa.com
Phone8882848004
Emailservice@oculususa.com
Phone8882848004
Emailservice@oculususa.com
Phone8882848004
Emailservice@oculususa.com
Phone8882848004
Emailservice@oculususa.com
Phone8882848004
Emailservice@oculususa.com
Phone8882848004
Emailservice@oculususa.com
Phone8882848004
Emailservice@oculususa.com
Phone8882848004
Emailservice@oculususa.com
Phone8882848004
Emailservice@oculususa.com
Phone8882848004
Emailservice@oculususa.com
Phone8882848004
Emailservice@oculususa.com
Phone8882848004
Emailservice@oculususa.com
Phone8882848004
Emailservice@oculususa.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100850040295818 [Primary]

FDA Product Code

QTODigital Visual Acuity Test

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-01-02
Device Publish Date2023-12-25

Devices Manufactured by The Hilsinger Company Parent LLC

00850040295818 - OCULUS Easyfield VR2024-01-02
00850040295818 - OCULUS Easyfield VR2024-01-02
00850040295016 - M&S Technologies VisiChart® Acuity Chart2022-07-14 M&S Technologies VisiChart® Acuity Chart
00850040295122 - M&S Technologies Smart System® Virtual Reality Headset System2022-07-14 M&S Technologies Smart System® Virtual Reality Headset System
00850040295139 - M&S Technologies Clinical Trial Suite®2022-07-14 M&S Technologies Clinical Trial Suite®
00850040295214 - M&S Technologies Melbourne Rapid Fields Device In-Clinic2022-07-14 M&S Technologies Melbourne Rapid Fields Device In-Clinic
00850040295351 - M&S Technologies ACUITYex2022-07-14 M&S Technologies ACUITYex
00850040295559 - M&S Technologies Smart System® Standard2022-07-14 M&S Technologies Smart System® Standard
00850040295047 - M&S Technologies Smart System® 20/202022-07-14 M&S Technologies Smart System® 20/20

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