GUDIDData
gudid Primary ID: 56353

Halyard (UDI 56353)

Manufactured by OWENS & MINOR DISTRIBUTION, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Halyard - Primary ID 56353

Device Regulatory Overview

The Halyard (Model/Catalog Number: 56353) is a medical device manufactured by OWENS & MINOR DISTRIBUTION, INC.. This product is indexed under FDA Product Code / Category Classification KGN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
56353
Product Code / EMDN
KGN
Device Name
HALYARD Collagen Dressing 7x7IN
Database Sync Date
2026-08-09 09:16:24

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 Halyard?

The registered manufacturer of record for Halyard is OWENS & MINOR DISTRIBUTION, INC..

What is the Primary UDI-DI identifier for Halyard?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 56353.

What classification code is assigned to this device?

This device is registered under product classification code KGN.

Programmatic Export

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

JSON API Endpoint