GUDIDData
eudamed_udi Primary ID: +G072RO56420R0W

Lowman-Hoglund Bone Holding Forceps, 20cm (UDI +G072RO56420R0W)

Manufactured by Rhein Enterprises (Pvt) Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lowman-Hoglund Bone Holding Forceps, 20cm - Primary ID +G072RO56420R0W

Device Regulatory Overview

The Lowman-Hoglund Bone Holding Forceps, 20cm (Model/Catalog Number: RO-564-20R) is a medical device manufactured by Rhein Enterprises (Pvt) Ltd. This product is indexed under FDA Product Code / Category Classification L03130401 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
RO-564-20R
Product Code / EMDN
L03130401
Device Name
Reusable, Stainless Steel, Non-Sterile Surgical Forceps
Database Sync Date
2026-08-09 16:28:57

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 Lowman-Hoglund Bone Holding Forceps, 20cm?

The registered manufacturer of record for Lowman-Hoglund Bone Holding Forceps, 20cm is Rhein Enterprises (Pvt) Ltd.

What is the Primary UDI-DI identifier for Lowman-Hoglund Bone Holding Forceps, 20cm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +G072RO56420R0W.

What classification code is assigned to this device?

This device is registered under product classification code L03130401.

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