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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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Substrate Buffer — 6 UDI-DI variants, IVDR

MD Atlas
biocyc Biotechnologie GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Substrate Buffer

42555978DETECCHR103P6

6 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: biocyc Biotechnologie GmbH & Co. KG

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 42555978DETECCHR103P6
Device name: Substrate Buffer
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Apr 4, 2025

Manufacturer & authorised representative

Manufacturer

Name: biocyc Biotechnologie GmbH & Co. KG
SRN: DE-MF-000031533
Country: Germany
Email: info@biocyc.de
Phone: +4933196782600

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JQZPM4XPTTTZRMYXMEJ29H39

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

005 PolyQ Stain DAB Substrate Buffer04255597806412
PolyQ Stain DAB Substrate Buffer04255597806368
PolyQ Stain DAB Substrate Buffer04255597806405
PolyQ Stain DAB Substrate Buffer04255597806399
PolyQ Stain DAB Substrate Buffer04255597806382
PolyQ Stain DAB Substrate Buffer04255597806375