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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

MAIRMATIC60 — Class IIa MDR by LUZZANI DENTAL SRL

MD Atlas
LUZZANI DENTAL SRL

EUDAMED last updated this device on May 6, 2026

MAIRMATIC60

805577605AIRMX

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LUZZANI DENTAL SRL
UDI-DI code: 08055776059952
Reference / catalog number: MAIRMATIC60

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View device family (Basic UDI)

Manufacturer information

Organization name: LUZZANI DENTAL SRL
SRN: IT-MF-000011279
Manufacturer status: Active

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MAIRMATIC805577605AIRMXOn the market MAMAIRMATICNA805577605AIRMXOn the market MAMAIRMATIC60NA805577605AIRMXOn the market SMASCG805577605SIRQROn the market SMATG805577605SIRQROn the market

Certificates

Certificate health across this manufacturer's portfolio.

IT344114Issued
Quality management systemNotified body: 1370Expiry: Jul 15, 2030

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08055776059952
Basic UDI-DI: 805577605AIRMX
Reference / catalog number: MAIRMATIC60
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: https://luzzani.it/en/download.asp?area=5
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08055776059952

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

Q019001SALIVA ASPIRATORS AND SALIVA ABSORBENTS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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