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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

MU3100ET — IVDR Class A IVDR by LABOINDUSTRIA Spa

MD Atlas
LABOINDUSTRIA Spa

EUDAMED last updated this device on Feb 19, 2026

MU3100ET

805669791CONTENITORIMUH2

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: LABOINDUSTRIA Spa
UDI-DI code: 80566979104768
Reference / catalog number: MU3100ET

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View device family (Basic UDI)

Manufacturer information

Organization name: LABOINDUSTRIA Spa
SRN: IT-MF-000029420
Manufacturer status: Active

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Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

Placed on the market in Italy; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 80566979104768
Basic UDI-DI: 805669791CONTENITORIMUH2
Reference / catalog number: MU3100ET
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Contenitore monouso 11.000ml per pezzi chirurgici, anatomici e istologici con etichetta ref/lotto sia sul contenitore che sul coperchio. Manico in plastica.
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)80566979104768

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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.

W05020104SAMPLES TRANSPORT, VASES

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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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.