VISUCONSULT 500 000000-2265-586

GUDID 04250668606618

N/A

Carl Zeiss Vision GmbH

Multidisciplinary medical image management software
Primary Device ID04250668606618
NIH Device Record Key02930b2c-9a79-48b7-b46f-203938e0eac2
Commercial Distribution StatusIn Commercial Distribution
Brand NameVISUCONSULT 500
Version Model Number000000-2265-586
Catalog Number000000-2265-586
Company DUNS333928146
Company NameCarl Zeiss Vision GmbH
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

Customer Support Contacts

Phone+1(423)598-2680
Emailjahmal.cannon@zeiss.com
Phone+1(423)598-2680
Emailjahmal.cannon@zeiss.com
Phone+1(423)598-2680
Emailjahmal.cannon@zeiss.com
Phone+1(423)598-2680
Emailjahmal.cannon@zeiss.com
Phone+1(423)598-2680
Emailjahmal.cannon@zeiss.com
Phone+1(423)598-2680
Emailjahmal.cannon@zeiss.com
Phone+1(423)598-2680
Emailjahmal.cannon@zeiss.com
Phone+1(423)598-2680
Emailjahmal.cannon@zeiss.com
Phone+1(423)598-2680
Emailjahmal.cannon@zeiss.com
Phone+1(423)598-2680
Emailjahmal.cannon@zeiss.com
Phone+1(423)598-2680
Emailjahmal.cannon@zeiss.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104250668606618 [Primary]

FDA Product Code

OUGMedical device data system

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-01-11
Device Publish Date2021-01-01

Devices Manufactured by Carl Zeiss Vision GmbH

04250668606045 - VISUSCREEN 100 Compact2023-06-07
04250668606052 - VISUCORE 500 Refractor2023-06-07
04250668606717 - i.Terminal 22021-02-01 N/A
04250668606618 - VISUCONSULT 5002021-01-11N/A
04250668606618 - VISUCONSULT 5002021-01-11 N/A
04250668606625 - i.Profiler plus2021-01-11 N/A
04250668606632 - ATLAS Review for i. Profiler plus2021-01-11 N/A
04250668606649 - i.Terminal mobile2021-01-11 N/A
04250668606663 - VISUFIT 1000 Platform2021-01-11 N/A

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.