GUDIDData
eudamed_udi Primary ID: +G072RY24224R0$

Shea Intra Oral Retractors 24.0cm With Cold Light Guide (UDI +G072RY24224R0$)

Manufactured by Rhein Enterprises (Pvt) Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Shea Intra Oral Retractors 24.0cm With Cold Light Guide - Primary ID +G072RY24224R0$

Device Regulatory Overview

The Shea Intra Oral Retractors 24.0cm With Cold Light Guide (Model/Catalog Number: RY-242-24R) is a medical device manufactured by Rhein Enterprises (Pvt) Ltd. This product is indexed under FDA Product Code / Category Classification L03140105 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
RY-242-24R
Product Code / EMDN
L03140105
Device Name
Reusable, Stainless Steel, Non-Sterile Surgical Retractors
Database Sync Date
2026-08-09 16:44:53

Full Regulatory Attributes

πŸ”’ 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 Shea Intra Oral Retractors 24.0cm With Cold Light Guide?

The registered manufacturer of record for Shea Intra Oral Retractors 24.0cm With Cold Light Guide is Rhein Enterprises (Pvt) Ltd.

What is the Primary UDI-DI identifier for Shea Intra Oral Retractors 24.0cm With Cold Light Guide?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +G072RY24224R0$.

What classification code is assigned to this device?

This device is registered under product classification code L03140105.

Programmatic Export

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

JSON API Endpoint