Uni-Gold Hiv Test Device — NAFDAC 03-1011: Is It Genuine? Uses, Alerts

Product: Uni-Gold Hiv Test Device
رقم NAFDAC: 03-1011
المادة الفعالة: HIV Test
التركيز: NA
الشكل: NA
حجم العبوة: 1 x 100; 1 x 20
Manufacturer: Not listed
Applicant (holder): Ash Biomedical Diagnostics Ltd
Approved: 2 Aug 2024
الحالة: Active View on NAFDAC ↗
التسجيل ساري حتى: 30 Jul 2029
تنبيهات منظمة الصحة العالمية: None found
Community reports: None
Times checked: 0

About the medicine: Hiv test: uses, dosage and brands worldwide

What we found

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. This is not medical advice. Always follow your doctor or pharmacist.

How to use Uni-Gold Hiv Test Device

ما تقوله النشرة الرسمية. إذا وصفه لك طبيب، فاتبع الوصفة. وإذا اختلفت نشرة عبوتك، فالأولوية لها.

لمن هو

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

كيف يُتناول وكم مرة

Connect bulb to solutions cup
Open top of cup, add approved Bronchodilator, close solutions cup
Squeeze bulb vigorously so visible vapor comes from the top
Breathe in slowly until approved Bronchodilator is gone
Disconnect bulb and follow Cleaning Instructions

Warnings

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

How to store it

Keep out of reach of children.

إذا نسيت جرعة

تناولها عندما تتذكر، إلا إذا اقترب موعد الجرعة التالية. عندها تخطَّ الجرعة المنسية. لا تتناول جرعتين معًا أبدًا للتعويض. راجع النشرة، فبعض الأدوية مختلفة.

ذكّرني بتناوله النشرة الرسمية كاملة

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2026-05-11.

Label for Uni-Gold Hiv Test Device, the active ingredient registered with NAFDAC.

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 …

Compare the brands and batch numbers in these notices with your pack, or enter your batch number above.

Check your pack of Uni-Gold Hiv Test Device

Add the expiry date on your pack for a full Trust Score.

اسم الدواء أو رقم التسجيل تاريخ الانتهاء على العبوة (اختياري) رقم التشغيلة (اختياري)

أين أنت؟ أو التقط صورًا للعبوة

تبقّت 3 عمليات تحقق مجانية اليوم Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

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 4 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.

How do I take Uni-Gold Hiv Test Device?

Follow your prescription or the leaflet in your pack. The official label says: Connect bulb to solutions cup. Open top of cup, add approved Bronchodilator, close solutions cup. Squeeze bulb vigorously so visible vapor comes from the top. Breathe in slowly until approved Bronchodilator is gone. Disconnect bulb and follow Cleaning Instructions.…

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 PillVera users, not medical advice. Report side effects to your doctor and to NAFDAC.