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Uni-Gold Hiv Test Device

NAFDAC Reg. No. 03-1011 · Drug

Registered with NAFDAC — registration activeAs of 5 November 2026 · synced automatically from official sources.
Product
Uni-Gold Hiv Test Device
NAFDAC number
03-1011
Active ingredient
HIV Test
Strength
NA
Form
NA
Pack size
1 x 100; 1 x 20
Manufacturer
Not listed
Applicant (holder)
Ash Biomedical Diagnostics Ltd
Approved
2 Aug 2024
Status
Active View on NAFDAC ↗
Registration valid to
30 Jul 2029
WHO alerts
None found
Community reports
None
Times checked
0

RxVerify commentary

  • Uni-Gold Hiv Test Device is on the NAFDAC register with an active registration (03-1011). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. Not medical advice — always follow your doctor or pharmacist.

What Uni-Gold Hiv Test Device is used for

From the official U.S. FDA label for Uni-Gold Hiv Test Device, the active ingredient registered with NAFDAC.

What it is used for

Please consult the use section of the OTC bronchodilator drug label approved for use with this device.

Purpose

Please consult the purpose section of the OTC bronchodilator drug label approved for use with this device.

Warnings

Please consult the warnings secton for the OTC bronchodilator drug label before use with this device.

General information only — not dosing advice. Always follow the leaflet in your pack and your doctor or pharmacist.

NAFDAC recall & alert notices

Public Alert No. 06/2026 – Alert on Revalidated Infant Formula (SMA Gold) Found on Sale12 Feb 2026 · nafdac.gov.ngThe National Agency for Food and Drug Administration and Control (NAFDAC) is alerting healthcare providers, caregivers, and the public about a report of a suspected revalidated SMA Gold First Infant Milk Formula (900g) found for sale in Kaduna State, Nigeria. The product allegedly caused gastrointestinal distress in a …Public Alert: 019/2022 – Recall of All Batches of Hugold CBD Oil Products by Ireland Food safety Authority24 Mar 2022 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control (NAFDAC) is notifying the healthcare providers and the Public that Food safety Authority of Ireland has recall Hugold Cannabidiol (CBD) oil. Hugold CBD Oils were recalled because they were processed at a site where operations have not been approved by t…Public Alert No.023/2021 – Miracle8989 Issues Voluntary Nationwide Recall of PremierZen Gold 7000, PremierZen Platinum 8000 and MaxxZEN Platinum 12000, Due to Presence of Undeclared Sildenafil and Tadalafil8 Jul 2021 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control (NAFDAC) has been informed by the U.S Food and Drug Administration that Irving, Texas, Miracle8989 is voluntarily recalling all lots of PremierZen Gold 7000, PremierZen Platinum 8000 and MaxxZEN Platinum 12000, capsules to the consumer level. FDA analys…Public Alert No: 39/2020 – Alert on Happy Ducts Compress, Cord Care and Goldenseal Powder by WishGarden Herbs Due to Bacterial Contamination30 Dec 2020 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control (NAFDAC) has received information from the US FDA about voluntary recall of some lots of Happy Ducts Compress, Cord Care and Goldenseal Powder by WishGarden Herbs. The recall is due to a possible supply chain contamination with the bacteria Cronobacter …

Notices list affected brands and batch numbers — compare them with your pack. Enter your batch number above to check it automatically.

Check your pack of Uni-Gold Hiv Test Device

Add the expiry date printed on your pack for a full Trust Score — or look up uses, side effects and cheaper generics.

3 free checks left today · no signup Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About Uni-Gold Hiv Test Device

What is in Uni-Gold Hiv Test Device?

Uni-Gold Hiv Test Device contains HIV Test (NA), as na, according to its NAFDAC registration record.

Is Uni-Gold Hiv Test Device registered with NAFDAC?

Yes. Uni-Gold Hiv Test Device is listed on the NAFDAC register under registration number 03-1011, and its registration is active as of 5 November 2026.

Has Uni-Gold Hiv Test Device been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Uni-Gold Hiv Test Device in our automatically synced alert list.

How can I check that my pack of Uni-Gold Hiv Test Device is genuine?

Run a free authenticity scan with the NAFDAC number 03-1011, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

What is Uni-Gold Hiv Test Device used for?

Please consult the use section of the OTC bronchodilator drug label approved for use with this device. (Summarised from the official U.S. FDA label for Uni-Gold Hiv Test Device. Always follow your doctor or pharmacist.)

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Reviews are personal experiences from RxVerify users, not medical advice. Report side effects to your doctor and to NAFDAC.