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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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VELLO SINTETICO ANTIDECUBITO — 3 UDI-DI variants, MDR

MD Atlas
SAMAMED di Bresolin Federica

Data from EUDAMED, last updated May 30, 2026

VELLO SINTETICO ANTIDECUBITO

805572853DECUBITUS08ZU

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: SAMAMED di Bresolin Federica

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805572853DECUBITUS08ZU
Device name: —
Device model: VELLO SINTETICO ANTIDECUBITO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: SAMAMED di Bresolin Federica
SRN: IT-MF-000032551
Country: Italy
Email: info@samamed.it
Phone: +39 3409952636

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KS7GH3AF6GDJ4184PGKA54VS

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

SYNTHETIC ANTIDECUBITUS FLEECE VA-10008055728530409
SYNTHETIC ANTIDECUBITUS FLEECE VA-5008055728530393
SYNTHETIC ANTIDECUBITUS HEEL AND ELBOW FLEECE VA-GT08055728530416