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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

M-LILYUM — Class IIb MDR by Metaltronica SpA

MD Atlas
Metaltronica SpA

EUDAMED last updated this device on Feb 12, 2026

M-LILYUM

805240521ANALOGICGV

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Metaltronica SpA
UDI-DI code: 08052405210043
Reference / catalog number: M-LILYUM

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View device family (Basic UDI)

Manufacturer information

Organization name: Metaltronica SpA
SRN: IT-MF-000014684
Manufacturer status: Active

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	Aug 2, 2022	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08052405210043
Basic UDI-DI: 805240521ANALOGICGV
Reference / catalog number: M-LILYUM
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: LILYUM is a medical device intended to produce mammographic images of the breast that can be used for diagnosis. Its intended use is for two-dimensional diagnosis, screening, or for needle localization mammography in case of stereotactic biopsy.
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)08052405210043

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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.

Z11030201CONVENTIONAL MAMMOGRAPHY SYSTEMS

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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Related devices

M-HELI/2D805240521DIGITAL8HOn the market M-HELI/CMP805240521DIGITAL8HOn the market M-HELI/DBT805240521DIGITAL8HOn the market M-MAMMO 10805240521ANALOGICGVOn the market M-LILYUMB-08052405210043On the market

Certificates

Certificate health across this manufacturer's portfolio.

046/MDRIssued
Quality management systemNotified body: 0051Expiry: Aug 1, 2027