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BinaxNOW COVID-19 Ag Positive Control Swab Pack

FDA UDI

Class N (US FDA UDI)

by Alere Scarborough, Inc.

Identity

Trade Name
BinaxNOW COVID-19 Ag Positive Control Swab Pack FDA UDI
Generic Name
SARS-CoV-2 antigen IVD, control FDA UDI
Device Name
Control swabs intended for use only with BinaxNOW COVID-19 Ag product manufactured by Abbott Diagnostics Scarborough, Inc. FDA UDI
Model / Reference
195-080 FDA UDI
Description
Control swabs intended for use only with BinaxNOW COVID-19 Ag product manufactured by Abbott Diagnostics Scarborough, Inc. FDA UDI

Identifiers

Primary DI / UDI-DI
10811877011306 FDA UDI
FDA Product Code
QKP FDA UDI
GMDN Term
SARS-CoV-2 antigen IVD, control 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

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, control

BinaxNOW COVID-19 Ag Positive Control Swab Pack by Alere Scarborough, Inc. — Class N — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as SARS-CoV-2 antigen IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9bef320c-753e-47d0-80d7-be1c972bedd7 33 fields · synced Jun 8, 2026