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Merocel Silicone Splint Kit - SFDA Registration ME0000000294SFDAA00089

Access comprehensive regulatory information for Merocel Silicone Splint Kit 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 ME0000000294SFDAA00089 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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Class I
ME0000000294SFDAA00089
Merocel Silicone Splint Kit
SFDA Registration: ME0000000294SFDAA00089
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Product 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
ME0000000294SFDAA00089
Authorization ID
GHTF-2018-1799
Status
Active
Expire Date
December 12, 2023
Manufacturer
Manufacturer Name
Medtronic XOMED, Inc
Model Information
Model ID(s)
400562
Product Accessories

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