Saudi Arabia SFDA registration ME0000003216SFDAA00229
FISHMOUTH DRILL GUIDE
Saudi Arabia·MD·DePuy Mitek A Johnson & Johnson Company·Class IActiveProduct 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
- Manufacturer Name
- DePuy Mitek A Johnson & Johnson Company
Model information
- Model ID(s)
- 213817
Product accessories
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About this record
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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