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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

8435814800010-SA-GR — Class I MDR by Fundación CARTIF

MD Atlas
Fundación CARTIF

EUDAMED last updated this device on Jun 20, 2025

8435814800010-SA-GR

843581480001058

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Fundación CARTIF
UDI-DI code: 08435814800010
Reference / catalog number: 8435814800010-SA-GR

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Manufacturer information

Organization name: Fundación CARTIF
SRN: ES-MF-000048251
Manufacturer status: Active

Market distribution

Primary placement in Spain; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 08435814800010
Basic UDI-DI: 843581480001058
Reference / catalog number: 8435814800010-SA-GR
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: The SELCA ANDIN is a motorized intelligent walker designed to provide assistance in walking, both indoors and outdoors. This advanced device allows users to improve their postural stability while walking, with minimal or no effort, thereby promoting greater independence in their movements.The walker includes safety features such as an automatic stop system, speed control, walking assistance adjustment, and fall detection and emergency situation alerts. In case of an emergency, the device can send an SMS alert to multiple contacts, including its geographical location in real-time. Additionally, the walker can also be operated remotely via Wifi.
Additional information URL: https://cartif.es/SELCA
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y120603WALKING FRAMES, 4 TIPS

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

8435814800027-SA-WH84358148000275ROn the market 8435814800003-SI-WH84358148000035BOn the market 8435814800034-SA-BL84358148000345NOn 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.