Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

Lumeen Manager — Class I MDR by LUMEEN

MD Atlas
LUMEEN

EUDAMED last updated this device on Sep 18, 2024

Lumeen Manager

3770025309DOPlatformQX

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LUMEEN
UDI-DI code: 03770025309071
Reference / catalog number: DOPlatform

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: LUMEEN
SRN: FR-MF-000022236
Manufacturer status: Active

Related devices

Lumeen3770025309LUMEEN-V4FBOn the market Lumeen3770025309LUMEEN-V2F7On the market Lumeen3770025309LUMEEN-V3F9On the market Lumeen3770025309LUMEEN-V4FBOn 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 Belgium; available across 3 countries total.

Country	On market since	Until
BelgiumPrimary placement		Still on market
France		Still on market
Luxembourg		Still on market

Device identification

Trade name: Lumeen Manager
UDI-DI code: 03770025309071
Basic UDI-DI: 3770025309DOPlatformQX
Reference / catalog number: DOPlatform
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: Le logiciel DOPlatform est un MDM (Gestionnaire de Dispositifs Mobiles) qui sécurise les appareils hôtes, restreint l'accès aux fonctions essentielles, accorde au logiciel Lumeen un accès indirect à certaines fonctionnalités d'Android, et gère les mises à jour du logiciel Lumeen.
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