Quick Answer
NAFDAC registration is required for medical products — devices, drugs, and related health products — imported into Nigeria. Products must be registered before the first commercial import, involving documentation, testing, and review, with the NAFDAC number displayed on packaging. Plan registration well ahead of shipment.
NAFDAC for Medical Imports
- Required for medical devices, drugs, and health products
- Must be registered before first commercial import
- Involves documentation, testing, and agency review
- NAFDAC number displayed on packaging
NAFDAC is separate from SONCAP and from device certification like CE/FDA. See our importing to Nigeria guide and NAFDAC overview.
Key Takeaways
- NAFDAC required for medical products in Nigeria.
- Register before first commercial import.
- Involves documentation, testing, and review.
- Separate from SONCAP and CE/FDA.
Frequently Asked Questions
Do medical products need NAFDAC registration for Nigeria?
Yes. Medical devices, drugs, and related health products must be NAFDAC-registered before the first commercial import into Nigeria, with the NAFDAC number on packaging.
How long does NAFDAC registration take?
It involves documentation, testing, and agency review and takes time, so it must be planned well before the first shipment. Timelines vary by product type.
Is NAFDAC the same as CE or FDA?
No. NAFDAC is Nigeria's national registration. A device may also hold CE or FDA clearance, but those do not replace NAFDAC registration for the Nigerian market.
Is NAFDAC the same as SONCAP?
No. NAFDAC covers health products (devices, drugs); SONCAP covers other regulated goods. A medical product generally needs NAFDAC, not SONCAP.
Can Plutonia help with NAFDAC for medical products?
Yes. Plutonia coordinates NAFDAC registration for medical products with local partners before shipment. Submit your product details to start.