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

P40001 — Class I MDR by Improving Mobility…

MD Atlas
Improving Mobility Development SL

EUDAMED last updated this device on Apr 4, 2025

P40001

436584K40000AEL

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Improving Mobility Development SL
UDI-DI code: 08436584360599
Reference / catalog number: P40001

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: Improving Mobility Development SL
SRN: ES-MF-000010985
Manufacturer status: Active

Related devices

K10010436584K10000BDFOn the market K10009436584K10000BDFOn the market K30036436584K30000AE7On the market K40050436584K40000AELOn the market K40014436584K40000AELOn 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 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: 08436584360599
Basic UDI-DI: 436584K40000AEL
Reference / catalog number: P40001
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: Se trata de un cojín diseñado para colocar en el asiento o el respaldo de sillas de ruedas. Su interior está compuesto por una capa de 3 cm de espuma viscoelástica y una capa de 5 cm de espuma de poliuretano; mientras que su exterior consiste en una funda antibacterias, antihongos y antiácaros que a su vez es lavable, transpirable, impermeable y antideslizante. El cojín previene la aparición de escaras o úlceras de decúbito propias de los cuerpos que permanecen inmóviles durante un largo periodo de tiempo y soporta un peso máximo de usuario de 100 kg. Sus dimensiones son 42 x 42 x 8 cm (largo x ancho x alto) y está disponible en dos colores, negro y azul
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08030102NON-ACTIVE ANTI-DECUBITUS MEDICAL CUSHIONS

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