Pure Global

DITHMAR CRVO-RON KNIFE - SFDA Registration ME0000003714SFDAA00024

Access comprehensive regulatory information for DITHMAR CRVO-RON 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 ME0000003714SFDAA00024 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.

Free Database
Powered by Pure Global AI
SFDA Official Data
Class I
ME0000003714SFDAA00024
DITHMAR CRVO-RON KNIFE
SFDA Registration: ME0000003714SFDAA00024
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Information

Instruments to cut or incise in different variants and designs

Product Use

Used to cut and incise in central retinal vein occlusion (CRVO) surgery

Device Classification
Risk Class
Class I
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000003714SFDAA00024
Authorization ID
MDMA-1-2017-1487
Status
Active
Expire Date
May 26, 2024
Manufacturer
Manufacturer Name
GEUDER AG
Model Information
Model ID(s)
G-12220
Product Accessories

[]