Hwang-Latina 5.0 Bar SLT Gonio Laser Lens w/ Flange

GUDID 00630238114295

OCULAR INSTRUMENTS, INC.

Gonioscope
Primary Device ID00630238114295
NIH Device Record Key627f89b3-4148-4680-9d92-3de03ca799a4
Commercial Distribution StatusIn Commercial Distribution
Brand NameHwang-Latina 5.0 Bar SLT Gonio Laser Lens w/ Flange
Version Model NumberOHLSLTF-IR
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
GS100630238114295 [Primary]
GS100630238114332 [Direct Marking]

FDA Product Code

HKSPrism, Gonioscopic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00630238114295]

High-level Disinfectant


[00630238114295]

High-level Disinfectant


[00630238114295]

High-level Disinfectant


[00630238114295]

High-level Disinfectant


[00630238114295]

High-level Disinfectant


[00630238114295]

High-level Disinfectant


[00630238114295]

High-level Disinfectant


[00630238114295]

High-level Disinfectant


[00630238114295]

High-level Disinfectant


[00630238114295]

High-level Disinfectant


[00630238114295]

High-level Disinfectant


[00630238114295]

High-level Disinfectant


[00630238114295]

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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