Saudi Arabia SFDA registration ME0000006290SFDAA00129
Landolt Raspatory
Saudi Arabia·Medical Device·RZ-Medizintechnik GmbH·Class IActiveProduct information
A surgical instrument to file or shape a bone or cartilage.
Product use
It is a tool or device which is designed for performing specific actions or carrying out desired effects during a surgery or operation.
Device classification
- Risk Class
- Class I
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000006290SFDAA00129
- Authorization ID
- GHTF-2021-0169
- Status
- Active
- Expire Date
- January 20, 2024
Manufacturer
- Manufacturer Name
- RZ-Medizintechnik GmbH
Model information
- Model ID(s)
- 210-439-175
Product accessories
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About this record
Access comprehensive regulatory information for Landolt Raspatory 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 ME0000006290SFDAA00129 and manufactured by RZ-Medizintechnik GmbH.
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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