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ACON SARS-CoV-2 IgG/IgM Rapid Test

FDA UDI

Class N (US FDA UDI)

by ACON Laboratories, Inc.

Identity

Trade Name
ACON SARS-CoV-2 IgG/IgM Rapid Test FDA UDI
Generic Name
SARS-CoV-2 immunoglobulin G (IgG)/IgM antibody IVD, kit, rapid ICT, clinical FDA UDI
Device Name
Test Cassettes (25), 2.5mL Buffer Bottles (2), Droppers (25) FDA UDI
Model / Reference
L031-11711 FDA UDI
Description
Test Cassettes (25), 2.5mL Buffer Bottles (2), Droppers (25) FDA UDI

Identifiers

Catalog Number
200979 FDA UDI
Primary DI / UDI-DI
00682607200979 FDA UDI
FDA Product Code
QKO FDA UDI
GMDN Term
SARS-CoV-2 immunoglobulin G (IgG)/IgM antibody 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

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

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 immunoglobulin G (IgG)/IgM antibody IVD, kit, rapid ICT, clinical

ACON SARS-CoV-2 IgG/IgM Rapid Test by ACON Laboratories, Inc. — Class N — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as SARS-CoV-2 immunoglobulin G (IgG)/IgM antibody IVD, kit, rapid ICT, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6244f1ab-86ac-4a61-ae08-470358c4c934 36 fields · synced Jun 9, 2026