Organization name

SIEM NOVA SRL

SRN

IT-MF-000034107

Manufacturer status

Active

Primary placement in Italy; available across 32 countries total.

Trade name

ASPIRATORE CHIRURGICO MOD. DOMI AC

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.

08053435660372

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.

B-08053435660372

Reference / catalog number

66132

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 IIa

Applicable legislation

MDD [Directive 93/42/EEC on medical devices]

Status

On the market

Quantity

1

Additional product description

The DOMI AC vacuum pump is manufactured by SIEM - NOVA SRL and combines quality and maneuverability with safety and cleanliness features to ensure optimal operation. Equipped with antibacterial/viral FILTER and LIQUID STOP hydrophobic filter. It can be used with any jar available on the market because it has a UNIQUE JAR-STOP DEVICE composed of two silicone rubber straps.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• 30 LITRI / MINUTO

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

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

• Z120105SURGICAL MEDICAL ASPIRATORS

• Class IIa medical devices in EUDAMED

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