OSOM Ultra Strep A 5 Test Kit 148

GUDID 00742860100116

SEKISUI DIAGNOSTICS, LLC

Beta-haemolytic Group A Streptococcus antigen IVD, kit, immunochromatographic test (ICT), rapid Beta-haemolytic Group A Streptococcus antigen IVD, kit, immunochromatographic test (ICT), rapid Beta-haemolytic Group A Streptococcus antigen IVD, kit, rapid ICT, clinical Beta-haemolytic Group A Streptococcus antigen IVD, kit, rapid ICT, clinical Beta-haemolytic Group A Streptococcus antigen IVD, kit, rapid ICT, clinical Beta-haemolytic Group A Streptococcus antigen IVD, kit, rapid ICT, clinical Beta-haemolytic Group A Streptococcus antigen IVD, kit, rapid ICT, clinical Beta-haemolytic Group A Streptococcus antigen IVD, kit, rapid ICT, clinical Beta-haemolytic Group A Streptococcus antigen IVD, kit, rapid ICT, clinical
Primary Device ID00742860100116
NIH Device Record Key0703cd5a-385e-4d31-9e8d-db80c8c8fbf5
Commercial Distribution StatusIn Commercial Distribution
Brand NameOSOM Ultra Strep A 5 Test Kit
Version Model Number148
Catalog Number148
Company DUNS966812344
Company NameSEKISUI DIAGNOSTICS, LLC
Device Count5
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100742860100116 [Primary]
GS110742860100113 [Unit of Use]

FDA Product Code

GTYANTIGENS, ALL GROUPS, STREPTOCOCCUS SPP.

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-09-20

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