Organization name

Medica S.p.A.

SRN

IT-MF-000025691

Manufacturer status

Active

1 warning recorded — scroll inside the panel to see all entries.

• Caution

Primary placement in Italy; available across 32 countries total.

Trade name

AcuSmart 230V

UDI-DI code

Primary DI

The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.

08033772329484

Basic UDI-DI

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.

803377232M69G5

Reference / catalog number

M03879

Issuing entity

UDI issuing entities

Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.

GS1

Risk category

MDR risk classes

MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.

Class IIb

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

System for CRRT, Plasmapheresis, Hemoperfusion, CO₂ Removal

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

1 packaging level registered — each level carries its own UDI-DI.

• 08033772329484× 1 unitBase unit
  • 18033772329481× 1 unit

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• Z12090301HAEMOFILTRATION EQUIPMENT

• Class IIb medical devices in EUDAMED

No certificate specifically references this device's Basic UDI-DI.