eudamed_udi Primary ID: 05060446930434

Pro Headrest Medium, With swan neck vertical tube with ball mounting assembly (UDI 05060446930434)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Pro Headrest Medium, With swan neck vertical tube with ball mounting assembly (Model/Catalog Number: CS-PRO-M-SNB) is a medical device manufactured by Consolor Ltd. This product is indexed under FDA Product Code / Category Classification Y180980 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: CS-PRO-M-SNB
Product Code / EMDN: Y180980
Device Name: Pro Head Support
Database Sync Date: 2026-08-09 16:50:38

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 Pro Headrest Medium, With swan neck vertical tube with ball mounting assembly?

The registered manufacturer of record for Pro Headrest Medium, With swan neck vertical tube with ball mounting assembly is Consolor Ltd.

What is the Primary UDI-DI identifier for Pro Headrest Medium, With swan neck vertical tube with ball mounting assembly?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060446930434.

What classification code is assigned to this device?

This device is registered under product classification code Y180980.

Similar Classification Devices (Y180980)

Other Devices by Consolor Ltd

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