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Speedy Swab Rapid COVID-19 & FLU A+B Self-Test

FDA UDI

Class N (US FDA UDI)

by WatMIND USA

Identity

Trade Name
Speedy Swab Rapid COVID-19 & FLU A+B Self-Test FDA UDI
Generic Name
SARS-CoV-2 antigen IVD, kit, rapid ICT, clinical FDA UDI
Model / Reference
CARTON-RDB-4V-4VUS4C30-BIO FDA UDI

Identifiers

Primary DI / UDI-DI
60810172700071 FDA UDI
FDA Product Code
QKP FDA UDI
GMDN Term
SARS-CoV-2 antigen IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
N FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: SARS-CoV-2 antigen IVD, kit, rapid ICT, clinical

Speedy Swab Rapid COVID-19 & FLU A+B Self-Test by WatMIND USA — Class N — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as SARS-CoV-2 antigen IVD, kit, rapid ICT, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
WatMIND USA

Sources (1)

  • FDA UDI 5fac3da8-6539-4f3a-b08d-807e1928df00 33 fields · synced May 30, 2026