- Organization name
- UDI-DI code
- Reference / catalog number
DE-MF-000010089No 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.6PLUS1® Multilevel Serum Calibrator Set MassChrom® Steroid Panel 2 is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — General. Manufactured by Chromsystems Instruments + Chemicals GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Sep 17, 2026
B-04250317533425Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)04250317533425
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.
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.
Primary placement in Germany; available across 5 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | — | Still on market |
| Spain | — | Still on market |
| France | — | Still on market |
| Ireland | — | Still on market |
| Italy | — | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
04250317533425Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
B-0425031753342572039UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
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.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0101050301CALIBRATORS MULTICOMPONENT (CC)No certificate specifically references this device's Basic UDI-DI.
B-04250317552365On the market6PLUS1® Multilevel Serum Calibrator Set42503176200054On the market6PLUS1® Multilevel Serum Calibrator Set MassChrom®
Steroid Panel 1B-04250317533340On the market6PLUS1® Multilevel Urine Calibrator Set4250317807006FOn the market6PLUS1® Multilevel Urine Calibrator Set4250317960006ZOn the market6PLUS1® Multilevel Urine Calibrator SetB-04250317542342On the market