eudamed_udi
Primary ID: 05415168002219
CRP Gold Latex (UDI 05415168002219)
Manufactured by Diagam S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CRP Gold Latex - Primary ID 05415168002219
Device Regulatory Overview
The CRP Gold Latex (Model/Catalog Number: CPDGX-H00/ARC) is a medical device manufactured by Diagam S.A.. This product is indexed under FDA Product Code / Category Classification W01021109 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CPDGX-H00/ARC
- Product Code / EMDN
- W01021109
- Device Name
- CRP Gold Latex
- Database Sync Date
- 2026-08-09 16:48:33
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 Gold Latex?
The registered manufacturer of record for CRP Gold Latex is Diagam S.A..
What is the Primary UDI-DI identifier for CRP Gold Latex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05415168002219.
What classification code is assigned to this device?
This device is registered under product classification code W01021109.
Similar Classification Devices (W01021109)
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