Saudi Arabia SFDA registration ME0000000723SFDAA00229
Mountaineer™ OCT Spinal System Occipital Drill
Product information
Instruments for spine surgery
Product use
The device is intended for:
To promote fusion of the cervical spine and occipitocervico-thoracic junction (occiput-T3)
Device classification
- Risk Class
- Class I
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000000723SFDAA00229
- Authorization ID
- GHTF-2019-1848
- Status
- Active
- Expire Date
- June 02, 2022
Manufacturer
- Manufacturer Name
- DePuy Spine
Model information
- Model ID(s)
- 288310035
Product accessories
[{'tradeName': 'Mountaineer™ OCT Spinal System OC Univ. Joint Screwdriver', 'description': None, 'gmdn': '33968'}, {'tradeName': 'Mountaineer™ OCT Spinal System OC Univ. Joint Torque Driver', 'description': None, 'gmdn': '32865'}, {'tradeName': 'Mountaineer™ OCT Spinal System Occipital Drill Guide', 'description': None, 'gmdn': '35095'}, {'tradeName': 'Mountaineer™ OCT Spinal System Occipital Flex Shaft Drill', 'description': None, 'gmdn': '32390'}, {'tradeName': 'Mountaineer™ OCT Spinal System Occipital Plate Bender', 'description': None, 'gmdn': '44795'}, {'tradeName': 'Mountaineer™ OCT Spinal System Occipital Tap', 'description': None, 'gmdn': '17507'}, {'tradeName': 'Mountaineer™ OCT Spinal System Occipital Universal Joint Tap', 'description': None, 'gmdn': '17507'}]
About this record
Access comprehensive regulatory information for Mountaineer™ OCT Spinal System Occipital Drill 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 ME0000000723SFDAA00229 and manufactured by DePuy Spine.
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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