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TENACULUM HOOKLET, COTTLE - SFDA Registration ME0000001065SFDAA00972

Access comprehensive regulatory information for TENACULUM HOOKLET, COTTLE 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 ME0000001065SFDAA00972 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.

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SFDA Official Data
Class I
ME0000001065SFDAA00972
TENACULUM HOOKLET, COTTLE
SFDA Registration: ME0000001065SFDAA00972
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Product Information

Surgical Instruments

Product Use

Used for handling and retracting tissue.

Device Classification
Risk Class
Class I
Product Category
MD
Product Type
MD
Registration Information
Registration ID
ME0000001065SFDAA00972
Authorization ID
GHTF-2018-1751
Status
Active
Expire Date
May 26, 2024
Manufacturer
Model Information
Model ID(s)
37-686-16-07; 37-687-17-07
Product Accessories

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