eudamed_udi
Primary ID: 08806125680132
URiSCAN® 3 GPH strip (UDI 08806125680132)
Manufactured by YD Diagnostics CORP.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for URiSCAN® 3 GPH strip - Primary ID 08806125680132
Device Regulatory Overview
The URiSCAN® 3 GPH strip (Model/Catalog Number: U21) is a medical device manufactured by YD Diagnostics CORP.. This product is indexed under FDA Product Code / Category Classification W0101060204 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- U21
- Product Code / EMDN
- W0101060204
- Device Name
- URiSCAN® strip (Professional use)
- Database Sync Date
- 2026-08-09 19:08:59
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 URiSCAN® 3 GPH strip?
The registered manufacturer of record for URiSCAN® 3 GPH strip is YD Diagnostics CORP..
What is the Primary UDI-DI identifier for URiSCAN® 3 GPH strip?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08806125680132.
What classification code is assigned to this device?
This device is registered under product classification code W0101060204.
Similar Classification Devices (W0101060204)
Other Devices by YD Diagnostics CORP.
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