gudid Primary ID: ST02020A ROCK REFLEX FOR SPINE BOARDS

Spencer (UDI ST02020A ROCK REFLEX FOR SPINE BOARDS)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Spencer (Model/Catalog Number: ST02020A ROCK REFLEX FOR SPINE BOARDS) is a medical device manufactured by SPENCER ITALIA SRL. This product is indexed under FDA Product Code / Category Classification NZD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: ST02020A ROCK REFLEX FOR SPINE BOARDS
Product Code / EMDN: NZD
Device Name
Database Sync Date: 2026-08-09 09:04:28

Full Regulatory Attributes

🔒 Token Gated

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

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

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 ST02020A ROCK REFLEX FOR SPINE BOARDS.

What classification code is assigned to this device?

This device is registered under product classification code NZD.

Similar Classification Devices (NZD)

Other Devices by SPENCER ITALIA SRL

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint