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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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SISTEMI ANTIDECUBITO ATTIVI CLASSE I — 14 UDI-DI variants, MDR

MD Atlas
Service Med Srl

Data from EUDAMED, last updated May 30, 2026

SISTEMI ANTIDECUBITO ATTIVI CLASSE I

805572850MADSMIFK

14 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: Service Med Srl

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Device characteristics

Active device

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 805572850MADSMIFK
Device name: SISTEMI ANTIDECUBITO ATTIVI CLASSE I
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 14, 2026

Manufacturer & authorised representative

Manufacturer

Name: Service Med Srl
SRN: IT-MF-000021629
Country: Italy
Email: info@servicemed.it
Phone: +390456717441

Variants by status

UDI-DI variants

14 UDI-DI variants

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Applied filters

basicUdiUlid01KNRMD52KB230M9AWWCY8BM2A

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

S200008055728500600
S50EVPU08055728500143
EPA/6/0008055728500037
ESA/8/0008055728500006
SFLADPU08055728500082
SFAIRCL08055728500136
SFLBRNY08055728500112
SFLBAPU08055728500051
SFLBT08055728500129
SFLHIPU08055728500075
SFLIMPU08055728500099
SFLMIPU08055728500068
SFLPDPUU08055728500105
UAI/4/0008055728500013