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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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MYTHIC 3CRP Diluent — 2 UDI-DI variants, IVDR (Orphée SA)

MD Atlas
Orphée SA

Data from EUDAMED, last updated May 23, 2026

MYTHIC 3CRP Diluent

764014248HM3CRP-003CY

2 UDI-DI variants

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

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Orphée SA

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 764014248HM3CRP-003CY
Device name: MYTHIC 3CRP Diluent
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jan 30, 2026

Manufacturer & authorised representative

Manufacturer

Name: Orphée SA
SRN: CH-MF-000050926
Country: Switzerland
Email: ra@orphee-medical.com

Authorised representative

Name: PZ CORMAY Spółka Akcyjna
SRN: PL-AR-000026245
Country: Poland

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KG6Z7PTCHMD1Q7VSKEQWGEZD

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

HM3CRP-003-2007640142480174
HM3CRP-003-1007640142480167