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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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FAB rikasteliuos, 6 ml putki — 3 UDI-DI variants, IVDR

MD Atlas
Tammer BioLab Oy

Data from EUDAMED, last updated May 23, 2026

FAB rikasteliuos, 6 ml putki

643008010T037XR

3 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: Tammer BioLab Oy

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 643008010T037XR
Device name: FAB rikasteliuos, 6 ml putki
Device model: FAB6
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 30, 2022

Manufacturer & authorised representative

Manufacturer

Name: Tammer BioLab Oy
SRN: FI-MF-000010901
Country: Finland
Email: tilaukset@tammerbiolab.fi
Phone: +358505422210

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G3R639W1RFWRSNEJ0JPX0KXR

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

T29806430080101955
T03706430080100125
T03806430080100668