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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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MATERASSI ANTIDECUBITO NON ATTIVI… — 6 UDI-DI variants, MDR

MD Atlas
Service Med Srl

Data from EUDAMED, last updated May 30, 2026

MATERASSI ANTIDECUBITO NON ATTIVI CLASSE I

805572850MASSMIJU

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: Service Med Srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805572850MASSMIJU
Device name: MATERASSI ANTIDECUBITO NON ATTIVI CLASSE I
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 15, 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

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KP3K36EJ9X362Q0B89PJEAWN

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

M0PM14IM08055728500204
MM5000IM08055728500174
M3001FRB08055728500167
M5000IMB08055728500181
MM3001FR08055728500150
M00VEC0208055728500211