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EUDAMED last updated this device on Jun 4, 2026
425120430500001006HPMBT Easy T IVD Kit is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Bruker Daltonics GmbH & Co. KG. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
042512043294731916360(01)04251204329473
European Medical Device Nomenclature — the EU product classification assigned to this device.
W05030380MICROBIOLOGY DEVICES - ACCESSORIES28 warnings recorded — scroll inside the panel to see all entries.
CW444CW430CW401CW148CW043DE-MF-000024392The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
CW010CW038CW041CW057CW058CW076CW080CW081CW082CW084CW085CW087CW088CW106CW158CW167CW193CW194CW313CW416CW397CW291CW119Primary placement in Germany; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | — | Still on market |
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →IVDR risk classes
IVDR risk classes rank in-vitro diagnostic devices from lowest risk (Class A) to highest (Class D), based on the patient and public-health risk of a wrong result.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →No certificate specifically references this device's Basic UDI-DI.
No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.425120430100001004EPOn the marketMBT Biotarget 96 IVD425120430100001000EFOn the marketMBT Compass HT IVD425120430100001005EROn the marketMBT FAST Shuttle IVD425120430100001012ENOn the marketMBT Galaxy HCCA Matrix IVD425120430100001013EQOn the marketMBT HT Filamentous Fungi IVD Module425120430100001016EWOn the market