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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

Analyse d'Ordonnance et… — Class IIb MDR by Posos

MD Atlas
Posos

EUDAMED last updated this device on Jul 28, 2025

Analyse d'Ordonnance et Recommandation de Traitement

37700316490000000000001JV

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Posos
UDI-DI code: 03770031649000
Reference / catalog number: Analyse d'Ordonnance et Recommandation de Traitement

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Manufacturer information

Organization name: Posos
SRN: FR-MF-000032106
Manufacturer status: Active

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW010
For each functionality, an e-IFU is provided to the healthcare professional.
CW018
A Manual for instruction is provided in an electronic version in which Posos helps the healthcare professional to use the device.

Market distribution

Primary placement in Belgium; available across 2 countries total.

Country	On market since	Until
BelgiumPrimary placement	Jan 6, 2025	Jan 5, 2030
France	Jan 6, 2025	Jan 5, 2030

Device identification

Trade name: Analyse d'Ordonnance et Recommandation de Traitement
UDI-DI code: 03770031649000
Basic UDI-DI: 37700316490000000000001JV
Reference / catalog number: Analyse d'Ordonnance et Recommandation de Traitement
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)

Z129092VARIOUS INSTRUMENTS FOR FUNCTIONAL EXPLORATION AND THERAPEUTIC INTERVENTIONS - 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

Analyse et Recommandation de Posologie37700316490000000000002JXOn the market PososB-PososPBOn 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.