Four Mirror Karickhoff Gonio Laser Lens 18mm O.D.

GUDID 00630238031936

OCULAR INSTRUMENTS, INC.

Gonioscope
Primary Device ID00630238031936
NIH Device Record Key93e784ea-b8f0-4770-beb0-7e079c97f12e
Commercial Distribution StatusIn Commercial Distribution
Brand NameFour Mirror Karickhoff Gonio Laser Lens 18mm O.D.
Version Model NumberOJKA
Company DUNS046212387
Company NameOCULAR INSTRUMENTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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
GS100630238031936 [Primary]
GS100630238041270 [Direct Marking]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HKSPrism, Gonioscopic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00630238031936]

High-level Disinfectant


[00630238031936]

High-level Disinfectant


[00630238031936]

High-level Disinfectant


[00630238031936]

High-level Disinfectant


[00630238031936]

High-level Disinfectant


[00630238031936]

High-level Disinfectant


[00630238031936]

High-level Disinfectant


[00630238031936]

High-level Disinfectant


[00630238031936]

High-level Disinfectant


[00630238031936]

High-level Disinfectant


[00630238031936]

High-level Disinfectant


[00630238031936]

High-level Disinfectant


[00630238031936]

High-level Disinfectant


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-06-18
Device Publish Date2019-06-10

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