gudid
Primary ID: 500H
Quickie 500H (UDI 500H)
Manufactured by SUNRISE MEDICAL (US) LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Quickie 500H - Primary ID 500H
Device Regulatory Overview
The Quickie 500H (Model/Catalog Number: 500H) is a medical device manufactured by SUNRISE MEDICAL (US) LLC. This product is indexed under FDA Product Code / Category Classification ITI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 500H
- Product Code / EMDN
- ITI
- Device Name
- The QUICKIE Q500 H brings you a unique blend of rear-wheel drive and mid-wheel drive technology, delivering impressive outdoor performance coupled with indoor maneuverability. Bringing you the best of both worlds and exceptional comfort.
- Database Sync Date
- 2026-08-09 09:00:34
Full Regulatory Attributes
🔒 Token Gated
{
"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 Quickie 500H?
The registered manufacturer of record for Quickie 500H is SUNRISE MEDICAL (US) LLC.
What is the Primary UDI-DI identifier for Quickie 500H?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 500H.
What classification code is assigned to this device?
This device is registered under product classification code ITI.
Similar Classification Devices (ITI)
Other Devices by SUNRISE MEDICAL (US) LLC
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