Saudi Arabia SFDA registration ME0000005447SFDAA00204
ANCHORAGE Plate, Basal Osteotomy / Wedge
Saudi Arabia·Medical Device·Stryker GmbH·Class IIbActiveProduct 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
- ME0000005447SFDAA00204
- Authorization ID
- MDMA-1-2017-2034
- Status
- Active
- Expire Date
- May 26, 2027
Manufacturer
- Manufacturer Name
- Stryker GmbH
Model information
- Model ID(s)
- PLP50230; PLP53230; PLP54230; PLP55230
Product accessories
[]
About this record
Access comprehensive regulatory information for ANCHORAGE Plate, Basal Osteotomy / Wedge 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 ME0000005447SFDAA00204 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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