Covid 19 Testing Kit

GUDID 10860011770265

Covid 19 Testing Kit

Ditek Consulting, LLC

Multiple-genus respiratory virus antigen IVD, kit, rapid ICT, self-testing
Primary Device ID10860011770265
NIH Device Record Keya1dd2b77-2db8-4d77-a07a-f185e63f924e
Commercial Distribution StatusIn Commercial Distribution
Brand NameCovid 19 Testing Kit
Version Model Number141314
Company DUNS111296701
Company NameDitek Consulting, LLC
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 Usetrue
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
GS100860011770268 [Primary]
GS110860011770265 [Package]
Contains: 00860011770268
Package: Case [50 Units]
In Commercial Distribution

FDA Product Code

NNKContainer, Specimen Mailer And Storage, Non-Sterile

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-05-09
Device Publish Date2025-05-01

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