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DIAMOND KNIFE, TITANIUM, for R.K. - SFDA Registration ME0000003714SFDAA00002

Access comprehensive regulatory information for DIAMOND KNIFE, TITANIUM, for R.K. 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 ME0000003714SFDAA00002 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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SFDA Official Data
Class I
ME0000003714SFDAA00002
DIAMOND KNIFE, TITANIUM, for R.K.
SFDA Registration: ME0000003714SFDAA00002
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Product 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
ME0000003714SFDAA00002
Authorization ID
MDMA-1-2017-1487
Status
Active
Expire Date
May 26, 2024
Manufacturer
Manufacturer Name
GEUDER AG
Model Information
Model ID(s)
G-19345 G-31480
Product Accessories

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