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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

PHYSIO-F3 — Class IIa MDR by MARIOTTI & C. S.R.L.

MD Atlas
MARIOTTI & C. S.R.L.

EUDAMED last updated this device on Feb 3, 2026

PHYSIO-F3

805674633SURDEVTL

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MARIOTTI & C. S.R.L.
UDI-DI code: 08056746330392
Reference / catalog number: PHYSIO-F3

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View device family (Basic UDI)

Manufacturer information

Organization name: MARIOTTI & C. S.R.L.
SRN: IT-MF-000035061
Manufacturer status: Active

Related devices

PRAD-2805674633SURDEVTLOn the market MiniUNIKO C.L805674633SURDEVTLOn the market UNIKO PZ805674633SURDEVTLOn the market MiniUNIKO G805674633SURDEVTLOn the market MiniUNIKO PZ805674633SURDEVTLOn the market

Certificates

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.

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Feb 3, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08056746330392
Basic UDI-DI: 805674633SURDEVTL
Reference / catalog number: PHYSIO-F3
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: No additional information URL provided by the manufacturer.
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)08056746330392

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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.

Z12110101DENTAL TREATMENT UNITS

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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