gudid Primary ID: ST36456B C-MAXFIXING SYSTEM CERTIFIED 10G

Spencer (UDI ST36456B C-MAXFIXING SYSTEM CERTIFIED 10G)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Spencer (Model/Catalog Number: ST36456B C-MAXFIXING SYSTEM CERTIFIED 10G) is a medical device manufactured by SPENCER ITALIA SRL. This product is indexed under FDA Product Code / Category Classification INM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: ST36456B C-MAXFIXING SYSTEM CERTIFIED 10G
Product Code / EMDN: INM
Device Name
Database Sync Date: 2026-08-09 09:04:28

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 Spencer?

The registered manufacturer of record for Spencer is SPENCER ITALIA SRL.

What is the Primary UDI-DI identifier for Spencer?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ST36456B C-MAXFIXING SYSTEM CERTIFIED 10G.

What classification code is assigned to this device?

This device is registered under product classification code INM.

Similar Classification Devices (INM)

Other Devices by SPENCER ITALIA SRL

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