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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

LOGIPREN V2.4 — Class I MDD by Logiprem-F

MD Atlas
Logiprem-F

EUDAMED last updated this device on Aug 29, 2025

LOGIPREN V2.4

B-LOGIPREN.V2.4.BW

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Logiprem-F
UDI-DI code: D-LOGIPREN.V2.4.BW
Reference / catalog number: LOGIPREN V2.4

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Manufacturer information

Organization name: Logiprem-F
SRN: FR-MF-000003056
Manufacturer status: Active

Market distribution

Primary placement in France; available across 2 countries total.

Country	On market since	Until
FrancePrimary placement	May 24, 2021	Still on market
Spain	Jun 29, 2022	Still on market

Device identification

Trade name: LOGIPREN V2.4
UDI-DI code: D-LOGIPREN.V2.4.BW
Basic UDI-DI: B-LOGIPREN.V2.4.BW
Reference / catalog number: LOGIPREN V2.4
Issuing entity: EUDAMED

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Logiciel d'aide à la prescription, préparation, administration des médicaments dans les services de néonatologie et réanimation pédiatrique
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12040292GENERAL MEDICINE THERAPEUTIC TREATMENT INSTRUMENTS - MEDICAL DEVICE SOFTWARE

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

LOGIPREN V2.53770024749LOGIPRENV02G9On 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.