eudamed_udi
Primary ID: 08431673431341
CRP-ULTRA (UDI 08431673431341)
Manufactured by Spinreact S.A.U.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CRP-ULTRA - Primary ID 08431673431341
Device Regulatory Overview
The CRP-ULTRA (Model/Catalog Number: 43134) is a medical device manufactured by Spinreact S.A.U.. This product is indexed under FDA Product Code / Category Classification W01021109 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 43134
- Product Code / EMDN
- W01021109
- Device Name
- C-Reactive Protein (ultrasensitive)
- Database Sync Date
- 2026-08-09 16:29:47
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 CRP-ULTRA?
The registered manufacturer of record for CRP-ULTRA is Spinreact S.A.U..
What is the Primary UDI-DI identifier for CRP-ULTRA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08431673431341.
What classification code is assigned to this device?
This device is registered under product classification code W01021109.
Similar Classification Devices (W01021109)
Other Devices by Spinreact S.A.U.
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