Pure Global

Hex Remover - SFDA Registration ME0000000545SFDAA00076

Access comprehensive regulatory information for Hex Remover 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 ME0000000545SFDAA00076 and manufactured by MegaGen Implant Co., Ltd..

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.

Free Database
Powered by Pure Global AI
SFDA Official Data
Class I
ME0000000545SFDAA00076
Hex Remover
SFDA Registration: ME0000000545SFDAA00076
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Information

Dental Hex Remover Driver

Product Use

Designed to remove damaged structure containing Hex part such as Abutment Screw,

Device Classification
Risk Class
Class I
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000000545SFDAA00076
Authorization ID
GHTF-2016-0085
Status
Active
Expire Date
June 24, 2019
Manufacturer
Manufacturer Name
MegaGen Implant Co., Ltd.
Model Information
Model ID(s)
HSS,HSL
Product Accessories

[]