GUDIDData
gudid Primary ID: UE-LHPRO-32NT

Uterine ElevatOR PRO with Long Handle (UDI UE-LHPRO-32NT)

Manufactured by THE O R COMPANY PTY LTD

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Uterine ElevatOR PRO with Long Handle - Primary ID UE-LHPRO-32NT

Device Regulatory Overview

The Uterine ElevatOR PRO with Long Handle (Model/Catalog Number: UE-LHPRO-32NT) is a medical device manufactured by THE O R COMPANY PTY LTD. This product is indexed under FDA Product Code / Category Classification LKF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
UE-LHPRO-32NT
Product Code / EMDN
LKF
Device Name
Database Sync Date
2026-08-09 09:38:27

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 Uterine ElevatOR PRO with Long Handle?

The registered manufacturer of record for Uterine ElevatOR PRO with Long Handle is THE O R COMPANY PTY LTD.

What is the Primary UDI-DI identifier for Uterine ElevatOR PRO with Long Handle?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is UE-LHPRO-32NT.

What classification code is assigned to this device?

This device is registered under product classification code LKF.

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