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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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CLOTH ROLL — 98 UDI-DI variants, MDR (Eurosirel Spa)

MD Atlas
Eurosirel Spa

Data from EUDAMED, last updated May 30, 2026

CLOTH ROLL

8017990RCYJA

98 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: Eurosirel Spa

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8017990RCYJA
Device name: CLOTH ROLL
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 26, 2024

Manufacturer & authorised representative

Manufacturer

Name: Eurosirel Spa
SRN: IT-MF-000005982
Country: Italy
Email: m.lenti@eurosirel.it

Variants by status

UDI-DI variants

98 UDI-DI variants

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Applied filters

basicUdiUlid01HN315HTGBE22ZQ6AC76J66HZ

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

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RCT80128008053470801280
RCT114602 08017990114602
RCC12029008017990120290
RCT12031308017990120313
RCC12017708017990120177
RCE16384608017990163846
MONOPRIX - Sparadrap micro perforé03350033375826
RCE03767208000061037672
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RCT95936608056300959366
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RCT12002308017990120023
RCC12001608017990120016
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RCS120238 08017990120238
RCC120009 08017990120009
RCT120337 08017990120337
RCE12021408017990120214
RCC30791305604260307913
RCC30279605604260302796

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