Pure Global

RESECTION KNIFE - SFDA Registration ME0000001065SFDAA00766

Access comprehensive regulatory information for RESECTION KNIFE 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 ME0000001065SFDAA00766 and manufactured by Gebrueder Martin GmbH & Co. KG.

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.

Free Database
Powered by Pure Global AI
SFDA Official Data
Class I
ME0000001065SFDAA00766
RESECTION KNIFE
SFDA Registration: ME0000001065SFDAA00766
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Information

Surgical cutting instrument used to separate tissue.

Product Use

Used to cut or separate tissue.

Device Classification
Risk Class
Class I
Product Category
MD
Product Type
MD
Registration Information
Registration ID
ME0000001065SFDAA00766
Authorization ID
MDMA-1-2018-1747
Status
Active
Expire Date
May 26, 2024
Manufacturer
Model Information
Model ID(s)
10-560-06-07
Product Accessories

[]