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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

INU FORMS — Class I MDR by MOVE IN MED

MD Atlas
MOVE IN MED

EUDAMED last updated this device on Oct 22, 2024

INU FORMS

376037641INUFORMS9M

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MOVE IN MED
UDI-DI code: 03760376410007
Reference / catalog number: INU FORMS

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Manufacturer information

Organization name: MOVE IN MED
SRN: FR-MF-000026703
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Jan 1, 2018	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03760376410007
Basic UDI-DI: 376037641INUFORMS9M
Reference / catalog number: INU FORMS
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: INU FORMS est un outil de questionnaires en ligne permettant d'assurer le télésuivi de patients.
Additional information URL: https://www.moveinmed.com/
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.