gudid
Primary ID: 831727006453
HEELIFT GLIDE (UDI 831727006453)
Manufactured by POSITION HEALTH, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HEELIFT GLIDE - Primary ID 831727006453
Device Regulatory Overview
The HEELIFT GLIDE (Model/Catalog Number: 831727006453) is a medical device manufactured by POSITION HEALTH, LLC. This product is indexed under FDA Product Code / Category Classification FMP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 831727006453
- Product Code / EMDN
- FMP
- Device Name
- HEELIFT GLIDE Suspension Boot, Heel Protector, Convoluted Foam. Size Standard.
- Database Sync Date
- 2026-08-09 09:04:02
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 HEELIFT GLIDE?
The registered manufacturer of record for HEELIFT GLIDE is POSITION HEALTH, LLC.
What is the Primary UDI-DI identifier for HEELIFT GLIDE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 831727006453.
What classification code is assigned to this device?
This device is registered under product classification code FMP.
Similar Classification Devices (FMP)
Other Devices by POSITION HEALTH, LLC
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