GUDIDData
eudamed_udi Primary ID: +G072RI23202R0I

Kocher Retractor, 2 Prongs, Sharp, 22cm (UDI +G072RI23202R0I)

Manufactured by Rhein Enterprises (Pvt) Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kocher Retractor, 2 Prongs, Sharp, 22cm - Primary ID +G072RI23202R0I

Device Regulatory Overview

The Kocher Retractor, 2 Prongs, Sharp, 22cm (Model/Catalog Number: RI-232-02R) 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
RI-232-02R
Product Code / EMDN
L03140105
Device Name
Reusable, Stainless Steel, Non-Sterile Surgical Retractors
Database Sync Date
2026-08-09 16:29:36

Full Regulatory Attributes

πŸ”’ 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 Kocher Retractor, 2 Prongs, Sharp, 22cm?

The registered manufacturer of record for Kocher Retractor, 2 Prongs, Sharp, 22cm is Rhein Enterprises (Pvt) Ltd.

What is the Primary UDI-DI identifier for Kocher Retractor, 2 Prongs, Sharp, 22cm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +G072RI23202R0I.

What classification code is assigned to this device?

This device is registered under product classification code L03140105.

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