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CROSS-PROBE; ROUND HANDLE - SFDA Registration ME0000001065SFDAA00458

Access comprehensive regulatory information for CROSS-PROBE; ROUND HANDLE 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 ME0000001065SFDAA00458 and manufactured by Gebrueder Martin GmbH & Co. KG.

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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SFDA Official Data
Class I
ME0000001065SFDAA00458
CROSS-PROBE; ROUND HANDLE
SFDA Registration: ME0000001065SFDAA00458
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Product Information

Diagnostic surgical instruments

Product Use

Surgical instruments intended for processing, cleaning, care, disinfection and sterilization of the instruments.

Device Classification
Risk Class
Class I
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000001065SFDAA00458
Authorization ID
GHTF-2016-1399
Status
Active
Expire Date
March 22, 2019
Manufacturer
Model Information
Model ID(s)
43-348-10-07
Product Accessories

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