Multichem IA Plus IA310X

GUDID 05391523440431

TECHNO-PATH MANUFACTURING LIMITED

Multiple-type clinical chemistry analyte profile IVD, control
Primary Device ID05391523440431
NIH Device Record Key3c457021-bf4f-4285-9618-9c80f7c09493
Commercial Distribution StatusIn Commercial Distribution
Brand NameMultichem IA Plus
Version Model NumberIA310X
Catalog NumberIA310X
Company DUNS896365983
Company NameTECHNO-PATH MANUFACTURING LIMITED
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 Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS105391523440431 [Primary]

FDA Product Code

OHQMulti-Analyte Controls Unassayed

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-09-27
Device Publish Date2022-09-19

On-Brand Devices [Multichem IA Plus ]

05391523442190IA320X
05391523442183IA319X
0539152344204609339850190
0539152344203909339841190
0539152344202209339825190
05391523441988IA318X
05391523441971IA317X
05391523441964IA316X
05391523441957IA315MX
05391523441940IA315X
05391523441612IA310MX
0539152344074508P86-10
05391523440516IA313A
05391523440509IA312A
05391523440493IA311A
05391523440486IA310A
05391523440479IA313X
05391523440462IA312X
05391523440455IA311X
05391523440448IA314X
05391523440431IA310X
0539152344000405P76-10

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