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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

LGD 240 S — Class IIa MDR by Lipogems International…

MD Atlas
Lipogems International S.p.A.

EUDAMED last updated this device on May 8, 2026

LGD 240 S

8058773560001LGDU2

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Lipogems International S.p.A.
UDI-DI code: 08058773562142
Reference / catalog number: LGD 240 S

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View device family (Basic UDI)

Manufacturer information

Organization name: Lipogems International S.p.A.
SRN: IT-MF-000010159
Manufacturer status: Active

Related devices

LGD 120 B8058773560001LGDU2On the market LGD 240 B8058773560001LGDU2On the market LGD 240 O8058773560001LGDU2On the market LGD 120 S8058773560001LGDU2On the market LGD 60 O8058773560001LGDU2On 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

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: 08058773562142
Basic UDI-DI: 8058773560001LGDU2
Reference / catalog number: LGD 240 S
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)08058773562142

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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.

V0599CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER

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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