Saudi Arabia SFDA registration ME0000003714SFDAA00023
BARKAN GONIOTOMY KNIFE
Saudi Arabia·Medical Device·GEUDER AG·Class IActiveProduct information
Instruments to cut or incise in different variants and designs
Product use
Used to cut or incise during an ophthalmic surgery
Device classification
- Risk Class
- Class I
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000003714SFDAA00023
- Authorization ID
- MDMA-1-2017-1487
- Status
- Active
- Expire Date
- May 26, 2024
Manufacturer
- Manufacturer Name
- GEUDER AG
Model information
- Model ID(s)
- G-14210
Product accessories
[]
About this record
Access comprehensive regulatory information for BARKAN GONIOTOMY 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 ME0000003714SFDAA00023 and manufactured by GEUDER 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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