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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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Scintillation Tube volume 20 ml, 58 x… — 2 UDI-DI variants, IVDR

MD Atlas
R. Langenbrinck GmbH

Data from EUDAMED, last updated May 23, 2026

Scintillation Tube volume 20 ml, 58 x 25 mm

426235473Scinti4R

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: R. Langenbrinck GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426235473Scinti4R
Device name: Scintillation Tube volume 20 ml, 58 x 25 mm
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 17, 2026

Manufacturer & authorised representative

Manufacturer

Name: R. Langenbrinck GmbH
SRN: DE-MF-000025266
Country: Germany
Email: langenbrinck@langenbrinck.com
Phone: 0764196283600

Variants by status

UDI-DI variants

2 UDI-DI variants

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basicUdiUlid01KRTZAMQNH673234MPY010J2P

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

08-0050/FX04262354732372
08-0050/FE04262354732365