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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

Dosage check — Class IIb MDR by Synapse medicine

MD Atlas
Synapse medicine

EUDAMED last updated this device on Apr 4, 2025

Dosage check

37016244APosologie1CG

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Synapse medicine
UDI-DI code: 03701624400012
Reference / catalog number: Analyse de posologie

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Manufacturer information

Organization name: Synapse medicine
SRN: FR-MF-000009699
Manufacturer status: Active

Related devices

Adverse events37016244EfIndesirables1R9On the market Drug clinical alerts37016244AClinique1FZOn the market Drug interactions37016244InterMed16SOn the market Drug safety system37016244SySecuMed1BWOn the market Geriatric guidelines37016244RecoGeriatrie13BOn 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.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: Dosage check
UDI-DI code: 03701624400012
Basic UDI-DI: 37016244APosologie1CG
Reference / catalog number: Analyse de posologie
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: —
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
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Software identification