gudid
Primary ID: HM2533
F8X LACER ANKLE W/STAYS MD (UDI HM2533)
Manufactured by Hausmann Enterprises, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for F8X LACER ANKLE W/STAYS MD - Primary ID HM2533
Device Regulatory Overview
The F8X LACER ANKLE W/STAYS MD (Model/Catalog Number: HM2533) is a medical device manufactured by Hausmann Enterprises, LLC. This product is indexed under FDA Product Code / Category Classification ITW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HM2533
- Product Code / EMDN
- ITW
- Device Name
- Database Sync Date
- 2026-08-09 09:23:12
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 F8X LACER ANKLE W/STAYS MD?
The registered manufacturer of record for F8X LACER ANKLE W/STAYS MD is Hausmann Enterprises, LLC.
What is the Primary UDI-DI identifier for F8X LACER ANKLE W/STAYS MD?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HM2533.
What classification code is assigned to this device?
This device is registered under product classification code ITW.
Similar Classification Devices (ITW)
Other Devices by Hausmann Enterprises, LLC
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