BaaySCI Disposable Nasal Swab

GUDID 10891237001963

BaaySCI Disposable Nasal Swab . Specimen collection swab . Laboratory use

HOME AIDE DIAGNOSTICS, INC.

Nasopharyngeal swab Nasopharyngeal swab Nasopharyngeal swab Nasopharyngeal swab Nasopharyngeal swab Nasopharyngeal swab Nasopharyngeal swab Nasopharyngeal swab Nasopharyngeal swab Nasopharyngeal swab Nasopharyngeal swab Nasopharyngeal swab Nasopharyngeal swab Nasopharyngeal swab Nasopharyngeal swab Nasopharyngeal swab Oral/upper respiratory tract specimen collection swab Oral/upper respiratory tract specimen collection swab Oral/upper respiratory tract specimen collection swab Oral/upper respiratory tract specimen collection swab Oral/upper respiratory tract specimen collection swab Oral/upper respiratory tract specimen collection swab Oral/upper respiratory tract specimen collection swab Oral/upper respiratory tract specimen collection swab Oral/upper respiratory tract specimen collection swab Oral/upper respiratory tract specimen collection swab Oral/upper respiratory tract specimen collection swab Oral/upper respiratory tract specimen collection swab Oral/upper respiratory tract specimen collection swab Oral/upper respiratory tract specimen collection swab Oral/upper respiratory tract specimen collection swab
Primary Device ID10891237001963
NIH Device Record Keydb9ccc0a-7dfb-4949-9b13-1e45a09b7b56
Commercial Distribution StatusIn Commercial Distribution
Brand NameBaaySCI Disposable Nasal Swab
Version Model NumberBaayNS
Company DUNS783518983
Company NameHOME AIDE DIAGNOSTICS, INC.
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com
Phone888-703-3209
Emailinfo@diaago.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100891237001966 [Primary]
GS110891237001963 [Package]
Contains: 00891237001966
Package: Inner Carton [250 Units]
In Commercial Distribution
GS120891237001960 [Package]
Package: Outer Carton [20 Units]
In Commercial Distribution

FDA Product Code

KXGApplicator, Absorbent Tipped, Sterile

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-06-21
Device Publish Date2021-06-11

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