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Home / Drug A–Z / Mazimed IV Cannula

Mazimed IV Cannula

NAFDAC Reg. No. A3-101309 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Mazimed IV Cannula
NAFDAC number
A3-101309
Active ingredient
Cannula
Strength
NA
Form
NA
Pack size
50's
Manufacturer
Not listed
Applicant (holder)
Okeymazi Pharmaceutical Limited
Approved
1 Aug 2024
Status
Active View on NAFDAC ↗
Registration valid to
30 Jul 2029
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Mazimed IV Cannula is on the NAFDAC register with an active registration (A3-101309). 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 Mazimed IV Cannula

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

3 free checks left today Official sources: NAFDAC · WHO · U.S. FDA · Health Canada · NLM

About Mazimed IV Cannula

What is in Mazimed IV Cannula?

Mazimed IV Cannula contains Cannula (NA), as na, according to its NAFDAC registration record.

Is Mazimed IV Cannula registered with NAFDAC?

Yes. Mazimed IV Cannula is listed on the NAFDAC register under registration number A3-101309, and its registration is active as of 28 October 2026.

Has Mazimed IV Cannula been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Mazimed IV Cannula in our automatically synced alert list.

How can I check that my pack of Mazimed IV Cannula is genuine?

Run a free authenticity scan with the NAFDAC number A3-101309, 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.