eudamed_udi
Primary ID: 08806125621968
URiSCAN® Super Cassette ACR (UDI 08806125621968)
Manufactured by YD Diagnostics CORP.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for URiSCAN® Super Cassette ACR - Primary ID 08806125621968
Device Regulatory Overview
The URiSCAN® Super Cassette ACR (Model/Catalog Number: U83) is a medical device manufactured by YD Diagnostics CORP.. This product is indexed under FDA Product Code / Category Classification W01010901 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- U83
- Product Code / EMDN
- W01010901
- Device Name
- URiSCAN® strip (Professional use)
- Database Sync Date
- 2026-08-09 17:19:16
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® Super Cassette ACR?
The registered manufacturer of record for URiSCAN® Super Cassette ACR is YD Diagnostics CORP..
What is the Primary UDI-DI identifier for URiSCAN® Super Cassette ACR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08806125621968.
What classification code is assigned to this device?
This device is registered under product classification code W01010901.
Similar Classification Devices (W01010901)
Other Devices by YD Diagnostics CORP.
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