GUDIDData
eudamed_udi Primary ID: +G072RI23408R0Q

Kocher Retractor, 8 Prongs, Semi Sharp, 22cm (UDI +G072RI23408R0Q)

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, 8 Prongs, Semi Sharp, 22cm - Primary ID +G072RI23408R0Q

Device Regulatory Overview

The Kocher Retractor, 8 Prongs, Semi Sharp, 22cm (Model/Catalog Number: RI-234-08R) 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-234-08R
Product Code / EMDN
L03140105
Device Name
Reusable, Stainless Steel, Non-Sterile Surgical Retractors
Database Sync Date
2026-08-09 16:45:08

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 Kocher Retractor, 8 Prongs, Semi Sharp, 22cm?

The registered manufacturer of record for Kocher Retractor, 8 Prongs, Semi Sharp, 22cm is Rhein Enterprises (Pvt) Ltd.

What is the Primary UDI-DI identifier for Kocher Retractor, 8 Prongs, Semi Sharp, 22cm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +G072RI23408R0Q.

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