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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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Protection literie — 8 UDI-DI variants, MDR (MEDISTAR)

MD Atlas
MEDISTAR

Data from EUDAMED, last updated May 19, 2026

Protection literie

3665502LITERIXG

8 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: MEDISTAR

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3665502LITERIXG
Device name: Protection literie
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 3, 2025

Manufacturer & authorised representative

Manufacturer

Name: MEDISTAR
SRN: FR-MF-000042737
Country: France
Email: yoni@medistar.fr
Phone: +33 6 20 42 46 79

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01JQYRGY1J71AFB63AS98J0DMR

Format

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
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Drap de lit - 140x24003665502006898
Drap de transfert03665502007031
Drap fauteuil - 130x23003665502006980
Drap housse - 90x20003665502006867
Housse de couette - 110x21003665502006928
Housse de couette - 150x22003665502006959
Housse taie d'oreiller - 65x65+1003665502006836
Kit literie03665502007017