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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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Serum Calibrator & Serum Control for CDT — 2 UDI-DI variants, IVDR

MD Atlas
RECIPE Chemicals + Instruments GmbH

Data from EUDAMED, last updated May 23, 2026

Serum Calibrator & Serum Control for CDT

4049195CDTCTRLV8

2 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: RECIPE Chemicals + Instruments GmbH

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 4049195CDTCTRLV8
Device name: Serum Calibrator & Serum Control for CDT
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Version date: Oct 16, 2025

Manufacturer & authorised representative

Manufacturer

Name: RECIPE Chemicals + Instruments GmbH
SRN: DE-MF-000032553
Country: Germany
Email: info@recipe.de
Phone: +49 89 54 70 81 - 0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K7PF9XN788EEPZWY7C1ESVYM

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

ClinCal® Serum Calibrator Set lyophilised, for CDT04049195210135
ClinChek® Serum Control, lyophil., for CDT, Level I, II04049195210821