A revocation to this notice was published on 16 May 2023, Notice No. 2023-go2024.

Notice Type
Departmental
Notice Title

Notice of Authorisation to add Self-administered CLINITEST Rapid Antigen Test Product Codes Under the COVID-19 Public Health Response (Point-of-care Tests) Order 2021

Pursuant to clause 8 of the COVID-19 Public Health Response (Point-of-care Tests) Order 2021 (“Order”), I, the Director-General of Health, hereby authorise addition of the following self-test product codes for the CLINITEST® Rapid COVID-19 Antigen Test to the approved list of rapid antigen tests (RATs) to be used to test for SARS-CoV-2 or COVID-19.

The following product codes authorised are:

Catalogue

Catalogue Item Description

Pack Size

11556500

CLIN COV19Ag Self CE 1PK Case LP4 (EU)

Case (320x 1-Test Packs)

11556333

CLIN COV19Ag Self CE 1PK (kit SMN) (EU)

1-Test Pack

11556501

CLIN COV19Ag Self CE 1PK LP4 (printed on box) (EU)

1-Test Pack

11556328

CLIN COV19AgSelf CE 5PK Tube CASE LP2 (EU)

Case (170x 5-Test Packs)

11556327

CLIN COV19AgSelf CE 5PK Tube (kit SMN) (EU)

5-Test Pack

11556329

CLIN COV19AgSelf CE 5PK Tube LP2 (printed on box) (EU)

5-Test Pack

11561586

CLINITEST COV19 Ag Home (US) 1PK Case

Case (320x 1-Test Packs)

11561587

CLINITEST COV19 Ag Home (US) 1PK Kit

1-Test Pack

11556711

CLINITEST COV19 Ag Home (US) 5PK Case

Case (170x 5-Test Packs)

11556712

CLINITEST COV19 Ag Home (US) 5PK Kit

5-Test Pack


Dated this 13th day of January 2022.

ROBYN SHEARER, Acting Director-General of Health.