CASE SpeedySwab Rapid COVID_19 + Flu A&B Antigen Self-Test 4 Tests/Box

GUDID 10810172700038

WatMIND USA

SARS-CoV-2 antigen IVD, kit, rapid ICT, clinical
Primary Device ID10810172700038
NIH Device Record Keyf844a244-aa2c-4543-9b4c-268be36d7dbf
Commercial Distribution StatusIn Commercial Distribution
Brand NameCASE SpeedySwab Rapid COVID_19 + Flu A&B Antigen Self-Test 4 Tests/Box
Version Model NumberCASE SpeedySwab Rapid COVID_19 + Flu A&B Antigen S
Company DUNS117617770
Company NameWatMIND USA
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 Numbertrue
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS110810172700038 [Primary]

FDA Product Code

QYTOver-The-Counter Covid-19 Antigen Test

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-07-18
Device Publish Date2024-07-10

Devices Manufactured by WatMIND USA

50810172700081 - Speedy Swab Rapid COVID-19 & FLU A&B Self-Test 2024-09-09
50810172700098 - Speedy Swab Rapid COVID-19 & FLU A&B Self-Test 2024-09-09
00810172700079 - Speedy Swab Rapid COVID-19 & FLU A+B (4 Tests/Box)2024-08-16
00810172700086 - Speedy Swab Rapid COVID-19 & FLU A+B Self-Test (2 Tests/Box)2024-08-16
00810172700093 - Speedy Swab Rapid COVID-19 & FLU A+B Self-Test (1 Test/Box)2024-08-16
10810172700083 - RDB6-SAN-Speedy Swab Rapid COVID-19 & FLU A+B Self-Test (2 Tests/Box)2024-08-16
10810172700090 - RDB10-BIO-Speedy Swab Rapid COVID-19 & FLU A+B Self-Test (1 Test/Box)2024-08-16
20810172700080 - RDB6-BIO-Speedy Swab Rapid COVID-19 & FLU A+B Self-Test (2 Tests/Box)2024-08-16

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