Halyard (UDI 55755)
Manufactured by O&M HALYARD, INC.
Device Regulatory Overview
The Halyard (Model/Catalog Number: 55755) is a medical device manufactured by O&M HALYARD, INC.. This product is indexed under FDA Product Code / Category Classification EZS within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- 55755
- Product Code / EMDN
- EZS
- Device Name
- HALYARD* Skin Barrier Ostomy Powder 5 oz Puff Bottle
- 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 O&M HALYARD, INC..
What is the Primary UDI-DI identifier for Halyard?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 55755.
What classification code is assigned to this device?
This device is registered under product classification code EZS.
Similar Classification Devices (EZS)
Other Devices by O&M HALYARD, INC.
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