gudid Primary ID: SK10001E PROSKID-E YELLOW FRAME, BLACK SHEET

Spencer (UDI SK10001E PROSKID-E YELLOW FRAME, BLACK SHEET)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Spencer (Model/Catalog Number: SK10001E PROSKID-E YELLOW FRAME, BLACK SHEET) 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: SK10001E PROSKID-E YELLOW FRAME, BLACK SHEET
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 SK10001E PROSKID-E YELLOW FRAME, BLACK SHEET.

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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