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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

Apilife Medical — Class IIa MDR by Predict4health

MD Atlas
Predict4health

EUDAMED last updated this device on Apr 8, 2026

Apilife Medical

376032653SW00189

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Predict4health
UDI-DI code: 03760326530007
Reference / catalog number: Apilife Medical

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Manufacturer information

Organization name: Predict4health
SRN: FR-MF-000000601
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Apr 21, 2022	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03760326530007
Basic UDI-DI: 376032653SW00189
Reference / catalog number: Apilife Medical
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: Monitoring tool to facilitate patients' awareness and communication between patients and healthcare professionals by providing a customizable system of alerts. It is intended to be used by patients suffering from chronic diseases on the following organs: kidney, heart, lung, liver, bowel, and their healthcare professionals
Additional information URL: https://www.predict4health.com/user-manual
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12040182GENERAL MEDICINE DIAGNOSIS AND MONITORING INSTRUMENTS - SOFTWARE ACCESSORIES

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

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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.