SFDA Medical Device Registration
SFDA Approval in Oman
SFDA has issued various guidelines for the regulations of medical devices. if you want to place product in Saudi Arabia you need approval from MDMA I.e Medical Device Market Authorization. This is an electronic system and the aim of the system is to authorize medical devices once they comply with MDIR, which means Medical Device Interim Regulations.
What is SFDA Medical device Registration & regulations?
KSA (kingdom of Saudi Arabia) has been rated in the top 20 economically competitive countries in the world. SFDA is regulatory authority for medical devices and IVDs sold and distributed in Saudi Arabia. MDMA approval is needed to place your devices in Saudi Arabia market. SFDA reviews MDMA applications to prepare your submission carefully. Saudi Arabia updated their medical device regulations between 2019 to 2022, which affected device classification and changed concept and content of the MDMA (high risk application). Due to the changes and updated guidance previously approved devices, IVDs, medical supplies must comply with new regulations. As a medical device regulatory consultant, we always keep an eye on changes in regulations and current updates so that we can serve better to our clients.
How to Register With SFDA for Medical device registration and approval?
Following are the Steps to register your medical devices:
1. Medical Device Classification:
SFDA device classification | Risk class | MDR rule |
A | low | I |
A-sterile | Low-medium | Is |
A-Measuring functions | Low –medium | Im |
A-Reusable surgical instrument | Low-Medium | Ir |
B | Low-Medium | IIa |
C | Medium -High | IIb |
D | High | III |
The SFDA is also adopting the European medical device regulation IVDR:
SFDA medical devices class | Risk class | Classification rule |
A | Low | A |
B | Moderate | B |
C | Moderate-High | C |
D | High | D |
- Appointment of AR If Needed
Authorized representatives (AR) need to be registered and approved by SFDA. The legal manufacturers have two options one is to assign their local distributor and second one is to assign a consulting office who can provide more power and freedom to the legal manufacturer in market. Low risk medical devices don’t need AR.
- Apply to MDMA and Medical device registration:
Medical device manufacturers need to register their device with SFDA and obtain a certificate from MDMA (Medical Device Market Authorization) as per the MDIR (Medical Device Interim Regulations) Saudi Arabia. MDMA is needed for high-risk devices whereas low risk devices (non- sterile, non-measuring) don’t require prolonged MDMA.
How we help you with regulatory service?
If you are a new manufacturer or already active commercially, We team of Operon Strategist ensure compliance and efficient regulatory support through
- Providing Assistance in regulatory processes
- Providing Guidance for QMS establishments
- We help our clients in design and development & GAP analysis for products and companies.
- We create technical files for submission.
- Provide proper response and submission to SFDA enquiries
- Follow up till regulatory approval.
Feel free to ask any query related to this or to avail our services contact us.