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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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BLOTrix System 5 — 4 UDI-DI variants, IVDR (BioSciTec GmbH)

MD Atlas
BioSciTec GmbH

Data from EUDAMED, last updated May 23, 2026

BLOTrix System 5

42604972700022MW

4 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: BioSciTec GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42604972700022MW
Device name: BLOTrix System 5
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: BioSciTec GmbH
SRN: DE-MF-000007888
Country: Germany
Email: info@bioscitec.de
Phone: +4969 42082884

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS03PX7JDZN380PAE7SZVFB3

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

BLOTrix System 5/ BLOTrix Reader C1 L04260497270607
BLOTrix System 5/ BLOTrix Reader R2 L04260497270614
BLOTrix System 5/ BLOTrix Reader S104260497270621
recomScan System 5/ BLOTrix Reader S104260497270638