FORUM ASSIST match

GUDID 04049471070200

Carl Zeiss Meditec AG

Patient health record information system application software
Primary Device ID04049471070200
NIH Device Record Key26d28717-4a13-4bfc-a562-3ed4cd495dba
Commercial Distribution StatusIn Commercial Distribution
Brand NameFORUM ASSIST match
Version Model Number1
Company DUNS314594680
Company NameCarl Zeiss Meditec AG
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 Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104049471070200 [Primary]

FDA Product Code

NFJSystem, Image Management, Ophthalmic

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-04-21
Device Publish Date2021-04-13

On-Brand Devices [FORUM ASSIST match]

04049471000037This database entry covers UDI for SW Versions 1.4.1 and higher: (01)04049471000037(10)150 -> Ve
04049471100037This database entry covers UDI for SW Versions 1.4.1 and higher: (01)04049471000037(10)150-> Ver
040494710702001

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