GUDIDData
eudamed_udi Primary ID: 05060446930410

Pro Headrest Medium, With swan neck vertical tube mounting assembly, with cover (UDI 05060446930410)

Manufactured by Consolor Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pro Headrest Medium, With swan neck vertical tube mounting assembly, with cover - Primary ID 05060446930410

Device Regulatory Overview

The Pro Headrest Medium, With swan neck vertical tube mounting assembly, with cover (Model/Catalog Number: CS-PRO-M-SN) 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-SN
Product Code / EMDN
Y180980
Device Name
Pro Head Support
Database Sync Date
2026-08-09 16:59:44

Full Regulatory Attributes

🔒 Token Gated
{
    "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 mounting assembly, with cover?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060446930410.

What classification code is assigned to this device?

This device is registered under product classification code Y180980.

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