eudamed_udi
Primary ID: 05404035100653
Creatinine (UDI 05404035100653)
Manufactured by Cypress Diagnostics
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Creatinine - Primary ID 05404035100653
Device Regulatory Overview
The Creatinine (Model/Catalog Number: HB0080) is a medical device manufactured by Cypress Diagnostics. This product is indexed under FDA Product Code / Category Classification W01010207 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HB0080
- Product Code / EMDN
- W01010207
- Device Name
- Creatinine
- Database Sync Date
- 2026-08-09 16:47:59
Full Regulatory Attributes
๐ Token Gated
{
"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 Creatinine?
The registered manufacturer of record for Creatinine is Cypress Diagnostics.
What is the Primary UDI-DI identifier for Creatinine?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05404035100653.
What classification code is assigned to this device?
This device is registered under product classification code W01010207.
Similar Classification Devices (W01010207)
Other Devices by Cypress Diagnostics
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