gudid
Primary ID: 56179
Halyard (UDI 56179)
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 56179
Device Regulatory Overview
The Halyard (Model/Catalog Number: 56179) 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
- 56179
- Product Code / EMDN
- BWF
- Device Name
- Volumetric Incentive Spirometer 2500 mL with One Way Valve 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
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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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 56179.
What classification code is assigned to this device?
This device is registered under product classification code BWF.
Similar Classification Devices (BWF)
Other Devices by OWENS & MINOR DISTRIBUTION, INC.
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