Arigold I.V Cannula — NAFDAC A3-101097: Is It Genuine? Uses, Alerts

Ọja: Arigold I.V Cannula
Nọmba NAFDAC: A3-101097
Ohun elo ti nṣiṣe lọwọ: Cannula
Agbara: NA
Fọọmu: NA
Iwọn iṣakojọpọ: 1 x 50's (in hardboard pack)
Olupese: Ko ṣe atokọ
Olubẹwẹ (oluranlowo): Makki Pharmaceuticals Ltd
Ti fọwọsi: 3 Dec 2023
Ipò: Nṣiṣẹ Wo lórí NAFDAC ↗
Iforukọsilẹ wulo si: 29 Nov 2028
Tani o ṣe itaniji: Kosi ikankan ti a rii.
Ijabọ Agbegbe: Kò sí
Àwọn àyẹ̀wò àsìkò: 0

Nipa oogun naa: Cannula: uses, dosage and brands worldwide

What we found

Arigold I.V Cannula is on the NAFDAC register with an active registration (A3-101097). 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.

Check your pack of Arigold I.V Cannula

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

3 free checks left today Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Arigold I.V Cannula

What is in Arigold I.V Cannula?

Arigold I.V Cannula contains Cannula (NA), as na, according to its NAFDAC registration record.

Is Arigold I.V Cannula registered with NAFDAC?

Yes. Arigold I.V Cannula is listed on the NAFDAC register under registration number A3-101097, and its registration is active as of 3 November 2026.

Has Arigold I.V Cannula been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Arigold I.V Cannula in our automatically synced alert list.

How can I check that my pack of Arigold I.V Cannula is genuine?

Run a free authenticity scan with the NAFDAC number A3-101097, 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.

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