gudid
Primary ID: 831727007702
HEELIFT Classic (UDI 831727007702)
Manufactured by POSITION HEALTH, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HEELIFT Classic - Primary ID 831727007702
Device Regulatory Overview
The HEELIFT Classic (Model/Catalog Number: 831727007702) 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
- 831727007702
- Product Code / EMDN
- FMP
- Device Name
- HEELIFT Classic Suspension Boot, Heel Protector, Smooth Foam. Size Bariatric.
- 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 Classic?
The registered manufacturer of record for HEELIFT Classic is POSITION HEALTH, LLC.
What is the Primary UDI-DI identifier for HEELIFT Classic?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 831727007702.
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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