Saudi Arabia SFDA registration ME0000000294SFDAA00088
Merocel Silicone Splint
Saudi Arabia·MD·Medtronic XOMED, Inc·Class IActiveProduct information
Invasive Implants Device
Product use
Splint and Dressing for Epistaxis, post operative surgery and trauma to assist in tamponade and hemostasis
Device classification
- Risk Class
- Class I
- Product Category
- MD
- Product Type
- MD
Registration information
- Registration ID
- ME0000000294SFDAA00088
- Authorization ID
- GHTF-2018-1799
- Status
- Active
- Expire Date
- December 12, 2023
Manufacturer
- Manufacturer Name
- Medtronic XOMED, Inc
Model information
- Model ID(s)
- 400561
Product accessories
[]
About this record
Access comprehensive regulatory information for Merocel Silicone Splint in the Saudi Arabia medical device market through Pure Global AI's free database. This Class I device is registered with Saudi Arabia SFDA under registration number ME0000000294SFDAA00088 and manufactured by Medtronic XOMED, Inc.
This page provides complete registration details including product category (MD), manufacturer information, model details, and regulatory compliance data from the official Saudi Arabia SFDA medical device database. Pure Global AI offers free access to Saudi Arabia's complete medical device registry, helping global MedTech companies navigate SFDA regulations efficiently.
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