Four Mirror Mini Gonio Diagnostic Lens w/Large Ring

GUDID 00630238063272

OCULAR INSTRUMENTS, INC.

Gonioscope Gonioscope Gonioscope Gonioscope Gonioscope Gonioscope Gonioscope Gonioscope Gonioscope Gonioscope Gonioscope Gonioscope Gonioscope
Primary Device ID00630238063272
NIH Device Record Keyd7eaa137-cd66-4fca-b8c8-c94af1e0396f
Commercial Distribution StatusIn Commercial Distribution
Brand NameFour Mirror Mini Gonio Diagnostic Lens w/Large Ring
Version Model NumberO4GF-LR
Company DUNS046212387
Company NameOCULAR INSTRUMENTS, INC.
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 Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100630238061988 [Direct Marking]
GS100630238063272 [Primary]

FDA Product Code

HKSPrism, Gonioscopic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00630238063272]

High-level Disinfectant


[00630238063272]

High-level Disinfectant


[00630238063272]

High-level Disinfectant


[00630238063272]

High-level Disinfectant


[00630238063272]

High-level Disinfectant


[00630238063272]

High-level Disinfectant


[00630238063272]

High-level Disinfectant


[00630238063272]

High-level Disinfectant


[00630238063272]

High-level Disinfectant


[00630238063272]

High-level Disinfectant


[00630238063272]

High-level Disinfectant


[00630238063272]

High-level Disinfectant


[00630238063272]

High-level Disinfectant


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-06-19
Device Publish Date2019-06-11

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