Medmont Meridia Advanced Topographer Professional

GUDID 09349221000101

MEDMONT INTERNATIONAL PTY LTD

Corneal topography system
Primary Device ID09349221000101
NIH Device Record Key05524ee7-89ab-485b-a5eb-77877e3b4b39
Commercial Distribution StatusIn Commercial Distribution
Brand NameMedmont Meridia Advanced Topographer Professional
Version Model NumberProfessional
Company DUNS746137249
Company NameMEDMONT INTERNATIONAL PTY LTD
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 Numbertrue
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
GS109349221000101 [Primary]

FDA Product Code

MMQTopographer, Corneal, Ac-Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-09-22
Device Publish Date2022-09-14

Devices Manufactured by MEDMONT INTERNATIONAL PTY LTD

09349221000033 - Medmont Corneal Topographer E300 USB2022-09-22
09349221000040 - Medmont Automated Perimeter M700 USB2022-09-22
09349221000071 - Medmont Automated Perimeter DAC2022-09-22
09349221000088 - Visual Function Tester AT20P2022-09-22
09349221000101 - Medmont Meridia Advanced Topographer Professional2022-09-22
09349221000101 - Medmont Meridia Advanced Topographer Professional2022-09-22
09349221000118 - Medmont Meridia Advanced Topographer Classic2022-09-22

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