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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 IIa — 1 UDI-DI variant, MDR

MD Atlas
Service Med Srl

Data from EUDAMED, last updated May 30, 2026

SISTEMI ANTIDECUBITO ATTIVI CLASSE IIa

805572850MADSMIIA3N

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Service Med Srl

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Device characteristics

Active device

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 805572850MADSMIIA3N
Device name: SISTEMI ANTIDECUBITO ATTIVI CLASSE IIa
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
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

1 UDI-DI variant

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Applied filters

basicUdiUlid01G4D5AADA8N0DW96GHVVSAXAT

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

UP21/9/0008055728500020