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Cartilage knife - SFDA Registration ME0000005640SFDAA00116

Access comprehensive regulatory information for Cartilage 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 ME0000005640SFDAA00116 and manufactured by ASANUS Medizintechnik GmbH.

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
ME0000005640SFDAA00116
Cartilage knife
SFDA Registration: ME0000005640SFDAA00116
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Product Information

Reusable surgical instrument

Product Use

Surgical instruments serve as standard instruments for surgical interventions in general surgery. The instruments may only be used by adequately qualified medical staff for the intended use in the medical specialties.

Device Classification
Risk Class
Class I
Product Category
MD
Product Type
MD
Registration Information
Registration ID
ME0000005640SFDAA00116
Authorization ID
GHTF-2020-1707
Status
Active
Expire Date
August 23, 2023
Manufacturer
Model Information
Model ID(s)
MS0110, MS0110Y, MS0118, MS0130, MS0170, MS0180
Product Accessories

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