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Straumann® PURE Ceramic Implant - SFDA Registration ME0000000504SFDAA00462

Access comprehensive regulatory information for Straumann® PURE Ceramic Implant in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIb device is registered with Saudi Arabia SFDA under registration number ME0000000504SFDAA00462 and manufactured by Institut Straumann 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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Class IIb
ME0000000504SFDAA00462
Straumann® PURE Ceramic Implant
SFDA Registration: ME0000000504SFDAA00462
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Product Information

Endosseous Dental Implants

Product Use

The Straumann® PURE Ceramic Implant is suitable for the treatment of oral endosteal implantation in the upper and lower jaw and for the functional and esthetic oral rehabilitation of edentulous and partially edentulous patients (unless specific indications and limitations are specified).

Device Classification
Risk Class
Class IIb
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000000504SFDAA00462
Authorization ID
MDMA-1-2017-0072
Status
Active
Expire Date
June 15, 2025
Manufacturer
Manufacturer Name
Institut Straumann AG
Model Information
Model ID(s)
032.000S 032.001S 032.002S 032.003S
Product Accessories

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