GUDIDData
eudamed_udi Primary ID: +G072RAB13201R0J

Mod Martin Anoscope,22 mm Ø * 50 mm (UDI +G072RAB13201R0J)

Manufactured by Rhein Enterprises (Pvt) Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Mod Martin Anoscope,22 mm Ø * 50 mm - Primary ID +G072RAB13201R0J

Device Regulatory Overview

The Mod Martin Anoscope,22 mm Ø * 50 mm (Model/Catalog Number: RAB-132-01R) 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
RAB-132-01R
Product Code / EMDN
L03140105
Device Name
Reusable, Stainless Steel, Non-Sterile Surgical Retractors
Database Sync Date
2026-08-09 16:30:27

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 Mod Martin Anoscope,22 mm Ø * 50 mm?

The registered manufacturer of record for Mod Martin Anoscope,22 mm Ø * 50 mm is Rhein Enterprises (Pvt) Ltd.

What is the Primary UDI-DI identifier for Mod Martin Anoscope,22 mm Ø * 50 mm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +G072RAB13201R0J.

What classification code is assigned to this device?

This device is registered under product classification code L03140105.

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