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FISHMOUTH DRILL GUIDE - SFDA Registration ME0000003216SFDAA00229

Access comprehensive regulatory information for FISHMOUTH DRILL GUIDE 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 ME0000003216SFDAA00229 and manufactured by DePuy Mitek A Johnson & Johnson Company.

This page provides complete registration details including product category (MD), 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
ME0000003216SFDAA00229
FISHMOUTH DRILL GUIDE
SFDA Registration: ME0000003216SFDAA00229
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Product Information

Reusable Arthroscopy Instruments

Product Use

The replacement shear pins are for use in repair of a broken shear pin in one of the Reusable Arthroscopy Instruments covered by this package insert.

Device Classification
Risk Class
Class I
Product Category
MD
Product Type
MD
Registration Information
Registration ID
ME0000003216SFDAA00229
Authorization ID
GHTF-2018-1289
Status
Active
Expire Date
November 16, 2024
Manufacturer
Model Information
Model ID(s)
213817
Product Accessories

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