gudid Primary ID: CI-11088-R

General Instrument (UDI CI-11088-R)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The General Instrument (Model/Catalog Number: CI-11088-R) is a medical device manufactured by ALPHATEC SPINE, INC.. This product is indexed under FDA Product Code / Category Classification HWN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: CI-11088-R
Product Code / EMDN: HWN
Device Name: Modular OCT Shank Tip, 15, Right
Database Sync Date: 2026-08-09 09:14:12

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of General Instrument?

The registered manufacturer of record for General Instrument is ALPHATEC SPINE, INC..

What is the Primary UDI-DI identifier for General Instrument?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CI-11088-R.

What classification code is assigned to this device?

This device is registered under product classification code HWN.

Similar Classification Devices (HWN)

Other Devices by ALPHATEC SPINE, INC.

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