GUDIDData
gudid Primary ID: DYND12302

Medline (UDI DYND12302)

Manufactured by MEDLINE INDUSTRIES, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Medline - Primary ID DYND12302

Device Regulatory Overview

The Medline (Model/Catalog Number: DYND12302) is a medical device manufactured by MEDLINE INDUSTRIES, INC.. This product is indexed under FDA Product Code / Category Classification NNX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
DYND12302
Product Code / EMDN
NNX
Device Name
CATHETER,EXTERNAL,MALE,EXO,LTX,MED,30MM
Database Sync Date
2026-08-09 09:38:23

Full Regulatory Attributes

🔒 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 Medline?

The registered manufacturer of record for Medline is MEDLINE INDUSTRIES, INC..

What is the Primary UDI-DI identifier for Medline?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DYND12302.

What classification code is assigned to this device?

This device is registered under product classification code NNX.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint