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ANCHORAGE Plate, Lapidus / Cross Plate Step - SFDA Registration ME0000005447SFDAA00202

Access comprehensive regulatory information for ANCHORAGE Plate, Lapidus / Cross Plate Step 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 ME0000005447SFDAA00202 and manufactured by Stryker GmbH.

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
ME0000005447SFDAA00202
ANCHORAGE Plate, Lapidus / Cross Plate Step
SFDA Registration: ME0000005447SFDAA00202
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Product Information

Osteosynthesis Implants

Product Use

Indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion, and reconstruction of small bones of the hand, feet, wrist and ankles, finger and toes.

Device Classification
Risk Class
Class IIb
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000005447SFDAA00202
Authorization ID
MDMA-1-2017-2034
Status
Active
Expire Date
May 26, 2027
Manufacturer
Manufacturer Name
Stryker GmbH
Model Information
Model ID(s)
PLP29371; PLP29372
Product Accessories

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