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Status™ COVID-19 Antigen Rapid Test for Home Use

FDA UDI

Class N (US FDA UDI)

by Princeton Biomeditech Corp.

Identity

Trade Name
Status™ COVID-19 Antigen Rapid Test for Home Use FDA UDI
Generic Name
SARS-CoV-2 antigen IVD, kit, rapid ICT, self-testing FDA UDI
Device Name
Status™ COVID-19 Antigen for Home Use, 25 Test Kit FDA UDI
Model / Reference
BSP-512-25-00 FDA UDI
Description
Status™ COVID-19 Antigen for Home Use, 25 Test Kit FDA UDI

Identifiers

Catalog Number
BSP-512-025-00 FDA UDI
Primary DI / UDI-DI
10743816001645 FDA UDI
FDA Product Code
QKP FDA UDI
GMDN Term
SARS-CoV-2 antigen IVD, kit, rapid ICT, self-testing 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

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, kit, rapid ICT, self-testing

Status™ COVID-19 Antigen Rapid Test for Home Use by Princeton Biomeditech Corp. — 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, self-testing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 05049f4a-e996-416c-b347-3eb84c607475 36 fields · synced Jun 1, 2026