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Dovetail Meniscal Allograft Osteotome Blades - SFDA Registration ME0000001945SFDAA00287

Access comprehensive regulatory information for Dovetail Meniscal Allograft Osteotome Blades 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 ME0000001945SFDAA00287 and manufactured by Arthrex, Inc.

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
ME0000001945SFDAA00287
Dovetail Meniscal Allograft Osteotome Blades
SFDA Registration: ME0000001945SFDAA00287
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Product Information

A chisel-like one-piece manual surgical reusable instrumentย 

Product Use

Used to cut and or shape bone by percussion during an orthopaedic procedure

Device Classification
Risk Class
Class IIa
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000001945SFDAA00287
Authorization ID
MDMA-1-2019-1284
Status
Active
Expire Date
May 08, 2027
Manufacturer
Manufacturer Name
Arthrex, Inc
Model Information
Model ID(s)
AR-2960
Product Accessories

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