GUDIDData
gudid Primary ID: 56181

Halyard (UDI 56181)

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 56181

Device Regulatory Overview

The Halyard (Model/Catalog Number: 56181) is a medical device manufactured by OWENS & MINOR DISTRIBUTION, INC.. This product is indexed under FDA Product Code / Category Classification BWF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
56181
Product Code / EMDN
BWF
Device Name
Volumetric Incentive Spirometer 2500 mL Non Valved Polyurethane Clear Adult Use CA/12 Not made with Natural Rubber Latex Halyard
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
}
                            

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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 56181.

What classification code is assigned to this device?

This device is registered under product classification code BWF.

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