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VuePoint II Connector, Fixed Cross - SFDA Registration ME0000005437SFDAA00078

Access comprehensive regulatory information for VuePoint II Connector, Fixed Cross in the Saudi Arabia medical device market through Pure Global AI's free database. This Class II device is registered with Saudi Arabia SFDA under registration number ME0000005437SFDAA00078 and manufactured by NuVasive Inc..

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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Class II
ME0000005437SFDAA00078
VuePoint II Connector, Fixed Cross
SFDA Registration: ME0000005437SFDAA00078
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Product Information

Non sterile bone screw internal spinal fixation system

Product Use

An assembly of non-sterile implantable devices intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities, also used as an adjunct to spinal fusion [e.g., for degenerative disc disease (DDD)]. Otherwise known as a pedicle screw instrumentation system, it typically consists of a combination of anchors (e.g., bolts, hooks, pedicle screws or other types), interconnection mechanisms (incorporating nuts, screws, sleeves, or bolts), longitudinal members (e.g., plates, rods, plate/rod combinations), and/or transverse connectors. Non-sterile disposable devices associated with implantation may be included.

Device Classification
Risk Class
Class II
Product Category
MD
Product Type
MD
Registration Information
Registration ID
ME0000005437SFDAA00078
Authorization ID
MDMA-1-2019-5839
Status
Active
Expire Date
November 19, 2025
Manufacturer
Manufacturer Name
NuVasive Inc.
Model Information
Model ID(s)
8976128, 8976130, 8976132, 8976134, 8976136, 8976138
Product Accessories

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