- Role
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US-MF-000021651Piccolo Xpress is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Abaxis, Inc.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on May 27, 2022
++EABA11000000E7FPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
EABA11000000E1
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
3 warnings recorded — scroll inside the panel to see all entries.
Consult instructions for use before using the device
OTHER
OTHER
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 32 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | May 26, 2022 | Still on market |
| Austria | May 26, 2022 | Still on market |
| Belgium | May 26, 2022 | Still on market |
| Bulgaria | May 26, 2022 | Still on market |
| Cyprus | May 26, 2022 | Still on market |
| Czechia | May 26, 2022 | Still on market |
| Denmark | May 26, 2022 | Still on market |
| Estonia | May 26, 2022 | Still on market |
| EL | May 26, 2022 | Still on market |
| Spain | May 26, 2022 | Still on market |
| Finland | May 26, 2022 | Still on market |
| France | May 26, 2022 | Still on market |
| Croatia | May 26, 2022 | Still on market |
| Hungary | May 26, 2022 | Still on market |
| Ireland | May 26, 2022 | Still on market |
| Iceland | May 26, 2022 | Still on market |
| Italy | May 26, 2022 | Still on market |
| Liechtenstein | May 26, 2022 | Still on market |
| Lithuania | May 26, 2022 | Still on market |
| Luxembourg | May 26, 2022 | Still on market |
| Latvia | May 26, 2022 | Still on market |
| Malta | May 26, 2022 | Still on market |
| Netherlands | May 26, 2022 | Still on market |
| Norway | May 26, 2022 | Still on market |
| Poland | May 26, 2022 | Still on market |
| Portugal | May 26, 2022 | Still on market |
| Romania | May 26, 2022 | Still on market |
| Sweden | May 26, 2022 | Still on market |
| Slovenia | May 26, 2022 | Still on market |
| Slovakia | May 26, 2022 | Still on market |
| Türkiye | May 26, 2022 | Still on market |
| XI | May 26, 2022 | 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.
EABA11000000E1Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
++EABA11000000E7F1100-0000EUDI 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.
W0201010101CHEMISTRY ANALYSERS - LOW ROUTINE (Random access without ISE mode test/h <= 400)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.No certificate specifically references this device's Basic UDI-DI.