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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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Sticktite by OPTXEUROPE — 6 UDI-DI variants, MDR (DOSCA SRL)

MD Atlas
DOSCA SRL

Data from EUDAMED, last updated May 31, 2026

Sticktite by OPTXEUROPE

805520544LOOMCY

6 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: DOSCA SRL

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805520544LOOMCY
Device name: —
Device model: Sticktite by OPTXEUROPE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 9, 2026

Manufacturer & authorised representative

Manufacturer

Name: DOSCA SRL
SRN: IT-MF-000031334
Country: Italy
Email: d.scattolini@dosca.it

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KR6GTDHNB0XZX07PW59EQ3ZE

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

500408055205445004
501108055205445011
502808055205445028
503508055205445035
504208055205445042
505908055205445059