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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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Lenticular shaped inflatable cushion… — 3 UDI-DI variants, MDR

MD Atlas
LEDRAPLASTIC SPA

Data from EUDAMED, last updated May 30, 2026

Lenticular shaped inflatable cushion suitable for ergonomic sitting, proprioception activity and lower limb rehabilitation

8001698F3D06M1I1P0487

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: LEDRAPLASTIC SPA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8001698F3D06M1I1P0487
Device name: Lenticular shaped inflatable cushion suitable for ergonomic sitting, proprioception activity and lower limb rehabilitation
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 13, 2023

Manufacturer & authorised representative

Manufacturer

Name: LEDRAPLASTIC SPA
SRN: IT-MF-000021280
Country: Italy
Email: nevio.cosani@ledraplastic.it
Phone: +39 0432 975051

Variants by status

UDI-DI variants

3 UDI-DI variants

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Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
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Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Disc'o'Sit08001698089157
Disc’o’Sit08001698089119
Disc'o'Sit Jr.08001698089126