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Catheter, sterile - SFDA Registration ME0000003595SFDAA00238

Access comprehensive regulatory information for Catheter, sterile in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIa device is registered with Saudi Arabia SFDA under registration number ME0000003595SFDAA00238 and manufactured by KARL STORZ SE & Co. KG.

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 IIa
ME0000003595SFDAA00238
Catheter, sterile
SFDA Registration: ME0000003595SFDAA00238
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Product Information

Single-use exploration catheter

Product Use

Single-use exploration catheters are used in combination with a flexible endoscope to spray or inject a contrast medium/stain for the exploration of the papilla in the bile of the pancreatic ducts or the mucous membrane of suspected lesions in the gastrointestinal region

Device Classification
Risk Class
Class IIa
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000003595SFDAA00238
Authorization ID
GHTF-2018-1532
Status
Active
Expire Date
July 16, 2023
Manufacturer
Manufacturer Name
KARL STORZ SE & Co. KG
Model Information
Model ID(s)
110260-05 110261-10 110262-10
Product Accessories

[{'tradeName': 'Guide Wire, sterile', 'description': None, 'gmdn': ''}]