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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

Ordoclic LAP — Class I MDD by Ordoclik'

MD Atlas
Ordoclik'

EUDAMED last updated this device on Nov 17, 2023

Ordoclic LAP

B-OrdoclicLAPV2.065

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Ordoclik'
UDI-DI code: D-OrdoclicLAPV2.065
Reference / catalog number: Ordoclic LAP v2.0

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Manufacturer information

Organization name: Ordoclik'
SRN: FR-MF-000029214
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: Ordoclic LAP
UDI-DI code: D-OrdoclicLAPV2.065
Basic UDI-DI: B-OrdoclicLAPV2.065
Reference / catalog number: Ordoclic LAP v2.0
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: The Ordoclic LAP is a medical software application that aims at helping the prescription process from a health professional to a patient. This software does not aim at replacing the diagnosis process of a disease, nor at suggesting a drug for a given disease, nor at advertising any pharmaceutical company or drug. This tool does not replace any consultation and should be used during a consultation, whether it is in person, teleconsultation, or from a filled medical form.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

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

This device is not currently linked to any other device.

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.