GUDIDData
gudid Primary ID: 66020934

RENASYS G MEDIUM W/SOFT PORT (UDI 66020934)

Manufactured by SMITH & NEPHEW MEDICAL LIMITED

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RENASYS G MEDIUM W/SOFT PORT - Primary ID 66020934

Device Regulatory Overview

The RENASYS G MEDIUM W/SOFT PORT (Model/Catalog Number: 66020934) is a medical device manufactured by SMITH & NEPHEW MEDICAL LIMITED. This product is indexed under FDA Product Code / Category Classification OMP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
66020934
Product Code / EMDN
OMP
Device Name
RENASYS-G Gauze Dressing Kit with Soft Port Medium
Database Sync Date
2026-08-09 09:08:52

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 RENASYS G MEDIUM W/SOFT PORT?

The registered manufacturer of record for RENASYS G MEDIUM W/SOFT PORT is SMITH & NEPHEW MEDICAL LIMITED.

What is the Primary UDI-DI identifier for RENASYS G MEDIUM W/SOFT PORT?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 66020934.

What classification code is assigned to this device?

This device is registered under product classification code OMP.

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