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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

REM3AND — Class IIa MDR by Remedee Labs SA

MD Atlas
Remedee Labs SA

EUDAMED last updated this device on Jul 3, 2025

REM3AND

3770015737-REM3AND-MF

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Remedee Labs SA
UDI-DI code: 03770015737266
Reference / catalog number: REM3AND

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Manufacturer information

Organization name: Remedee Labs SA
SRN: FR-MF-000035489
Manufacturer status: Active

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: not provided
UDI-DI code: 03770015737266
Basic UDI-DI: 3770015737-REM3AND-MF
Reference / catalog number: REM3AND
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Accessory to the Remedee wristband, which communicates via Bluetooth
Additional information URL: https://novirem.remedee.com/manuel-utilisateur%20;%20https://fibrorem.remedee.com/manuel-utilisateur
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

N010180NEUROPHYSIOLOGY DEVICES - ACCESSORIES

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

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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.