gudid
Primary ID: UR206
Uresta (UDI UR206)
Manufactured by Resilia Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Uresta - Primary ID UR206
Device Regulatory Overview
The Uresta (Model/Catalog Number: UR206) is a medical device manufactured by Resilia Inc. This product is indexed under FDA Product Code / Category Classification HHW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- UR206
- Product Code / EMDN
- HHW
- Device Name
- Uresta Bladder Support Size 6
- Database Sync Date
- 2026-08-09 09:04:20
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 Uresta?
The registered manufacturer of record for Uresta is Resilia Inc.
What is the Primary UDI-DI identifier for Uresta?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is UR206.
What classification code is assigned to this device?
This device is registered under product classification code HHW.
Similar Classification Devices (HHW)
Other Devices by Resilia Inc
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