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RONGEUR KRAEMER STR.2X10MM 180MM - SFDA Registration ME0000000908SFDAA01894

Access comprehensive regulatory information for RONGEUR KRAEMER STR.2X10MM 180MM 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 ME0000000908SFDAA01894 and manufactured by Aesculap AG.

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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Class I
ME0000000908SFDAA01894
RONGEUR KRAEMER STR.2X10MM 180MM
SFDA Registration: ME0000000908SFDAA01894
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Product Information

neurosurgical rongeur

Product Use

The rongeurs are used for the ablation of soft tissue (e.g. intervertebral disk tissue, mucosa, ethmoidal cells, cell tissue, nucleus tissue, sequester material) in neurosurgery and spine surgery. The rongeurs cannot be used for the ablation of bones or adjacent bone structures, for which purpose Aesculap recommends using bone punches, because of their higher mechanical load capacity.

Device Classification
Risk Class
Class I
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000000908SFDAA01894
Authorization ID
MDMA-1-2019-3182
Status
Active
Expire Date
July 09, 2025
Manufacturer
Manufacturer Name
Aesculap AG
Model Information
Model ID(s)
FF820R
Product Accessories

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