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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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CYDXStrips — 4 UDI-DI variants, IVDR (Cypress Diagnostics)

MD Atlas
Cypress Diagnostics

Data from EUDAMED, last updated May 23, 2026

CYDXStrips

54040351CYDXStripsWH

4 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class B

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Manufacturer: Cypress Diagnostics

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 54040351CYDXStripsWH
Device name: CYDXStrips
Device model: Urine-10 - Urine-2GK - Urine-2GP - Urine-3
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Version date: Jan 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: Cypress Diagnostics
SRN: BE-MF-000000033
Country: Belgium
Email: cypress@diagnostics.be
Phone: +32 15 67 67 68

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KFFPYEBCGE7PJ5E4V2K0G8E4

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

CYDXStrips Urine 1005404035100608
CYDXStrips Urine 2GK05404035100615
CYDXStrips Urine 2GP05404035100622
CYDXStrips Urine 305404035100639