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Reflex ELC - SFDA Registration ME0000005736SFDAA00159

Access comprehensive regulatory information for Reflex ELC in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIb device is registered with Saudi Arabia SFDA under registration number ME0000005736SFDAA00159 and manufactured by Conmed Corporation.

This page provides complete registration details including product category (Medical Device), 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 IIb
ME0000005736SFDAA00159
Reflex ELC
SFDA Registration: ME0000005736SFDAA00159
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Product Information

Endoscopic Clip Applier with Titanium Clips 10mm

Product Use

It is intended for use in a variety of laparoscopic, gynecological, and endoscopic procedures to achieve hemostasis of vessels and other small tissue structures.

Device Classification
Risk Class
Class IIb
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000005736SFDAA00159
Authorization ID
GHTF-2018-2333
Status
Active
Expire Date
June 18, 2023
Manufacturer
Manufacturer Name
Conmed Corporation
Model Information
Model ID(s)
530
Product Accessories

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